Borohydride fuels in gas generant compositions

Information

  • Patent Grant
  • 5401340
  • Patent Number
    5,401,340
  • Date Filed
    Monday, January 10, 1994
    30 years ago
  • Date Issued
    Tuesday, March 28, 1995
    29 years ago
Abstract
A sodium-azide-free gas-generating composition includes an oxidizable borohydride fuel and an oxidizing agent containing oxygen and a metal. The fuel and the oxidizing agent are selected such that water vapor is produced upon reaction between the borohydride fuel and the oxidizing agent. Suitable oxidizing agents contain a metal and oxygen and are selected from a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, or mixtures thereof. The fuel and oxidizing agent are selected such that water vapor is the major gaseous combustion product.
Description

FIELD OF THE INVENTION
The present invention relates to gas generating compositions. More particularly, the present gas generant compositions comprise a borohydride fuel mixed with an appropriate oxidizing agent which, when combusted, generates a large quantity of water vapor.
BACKGROUND OF THE INVENTION
Gas generating chemical compositions are useful in a number of different contexts. One important use for such compositions is in the operation of "air bags." Air bags are gaining in acceptance to the point that many, if not most, new automobiles are equipped with such devices. Indeed, many new automobiles are equipped with multiple air bags to protect the driver and passengers.
In the context of automobile air bags, sufficient gas must be generated to inflate the device within a fraction of a second. Between the time the car is impacted in an accident, and the time the driver would otherwise be thrust against the steering wheel, the air bag must fully inflate. As a consequence, nearly instantaneous gas generation is required.
There are a number of additional important design criteria that must be satisfied. Automobile manufacturers and others have set forth the required criteria which must be met in detailed specifications. Preparing gas generating compositions that meet these important design criteria is an extremely difficult task. These specifications require that the gas generating composition produce gas at a required rate. The specifications also place strict limits on the generation of toxic or harmful gases or solids. Examples of restricted gases include carbon monoxide, carbon dioxide, NO.sub.x, SO.sub.x, and hydrogen sulfide. For example, carbon dioxide is limited to about 20 to 30 volume percent of the final gas volume produced.
The gas must be generated at a sufficiently and reasonably low temperature so that an occupant of the car is not burned upon impacting an inflated air bag. If the gas produced is overly hot, there is a possibility that the occupant of the motor vehicle may be burned upon impacting a deployed air bag. Accordingly, it is necessary that the combination of the gas generant and the construction of the air bag isolates automobile occupants from excessive heat. All of this is required while the gas generant maintains an adequate burn rate. In the industry, burn rates in excess of 0.5 inch per second (ips) at 1000 psi, and preferably in the range of from about 1.0 ips to about 1.2 ips at 1000 psi are generally desired.
Another related but important design criteria is that the gas generant composition produces a limited quantity of particulate materials. Particulate materials can interfere with the operation of the supplemental restraint system, present an inhalation hazard, irritate the skin and eyes, or constitute a hazardous solid waste that must be dealt with after the operation of the safety device. In the absence of an acceptable alternative, the production of irritating particulates is one of the undesirable, but tolerated aspects of the currently used sodium azide materials.
In addition to producing limited, if any, quantities of particulates, it is desired that at least the bulk of any such particulates be easily filterable. For instance, it is desirable that the composition produce a filterable slag to prevent the reaction products from escaping into the surrounding environment. This limits interference with the gas generating apparatus and the spreading of potentially harmful dust in the vicinity of the spent air bag which can cause lung, mucous membrane, and eye irritation to vehicle occupants and rescuers.
Both organic and inorganic materials have been proposed as possible gas generants. Such gas generant compositions include oxidizers and fuels which react at sufficiently high rates to produce large quantities of gas in a fraction of a second.
At present, sodium azide is the most widely used and currently accepted gas generating material. Sodium azide nominally meets industry specifications and guidelines. Nevertheless, sodium azide presents a number of persistent problems. Sodium azide is relatively toxic as a starting material, since its toxicity level as measured by oral rat LD.sub.50 is in the range of 45 mg/kg. Workers who regularly handle sodium azide have experienced various health problems such as severe headaches, shortness of breath, and other symptoms.
In addition, no matter what auxiliary oxidizer is employed, the combustion products from a sodium azide gas generant include caustic reaction products such as sodium oxide or sodium hydroxide. Molybdenum disulfide or sulfur have been used as oxidizers for sodium azide. However, use of such oxidizers results in toxic products such as hydrogen sulfide gas and corrosive materials such as sodium oxide and sodium sulfide. Rescue workers and automobile occupants have complained about both the hydrogen sulfide gas and the corrosive powder produced by the operation of sodium azide-based gas generants.
Increasing problems are also anticipated in relation to disposal of unused gas-inflated supplemental restraint systems, e.g. automobile air bags, in demolished cars. The sodium azide remaining in such supplemental restraint systems can leach out of the demolished car to become a water pollutant or toxic waste. Indeed, some have expressed concern that sodium azide might form explosive heavy metal azides or hydrazoic acid when contacted with battery acids following disposal.
Sodium azide-based gas generants are most commonly used for air bag inflation, but with the significant disadvantages of such compositions many alternative gas generant compositions have been proposed to replace sodium azide. Most of the proposed sodium azide replacements, however, fail to deal adequately with all of the criteria set forth above.
One group of chemicals that has received attention as a possible replacement for sodium azide includes tetrazoles and triazoles. These materials are generally coupled with conventional oxidizers such as KNO.sub.3 and Sr(NO.sub.3).sub.2. Some of the tetrazoles and triazoles that have been specifically mentioned include 5-aminotetrazole, 3-amino-1,2,4-triazole, 1,2,4-triazole, 1H-tetrazole, bitetrazole and several others. However, because of poor ballistic properties and high gas temperatures, none of these materials has yet gained general acceptance as a sodium azide replacement.
It will be appreciated, therefore, that there are a number of important criteria for selecting gas generating compositions for use in automobile supplemental restraint systems. For example, it is important to select starting materials that are not toxic. At the same time, the combustion products must not be toxic or harmful. In this regard, industry standards limit the allowable amounts of various gases produced by the operation of supplemental restraint systems.
It would, therefore, be a significant advance to provide compositions capable of generating large quantities of gas that would overcome the problems identified in the existing art. It would be a further advance to provide a gas generating composition which is based on substantially nontoxic starting materials and which produces substantially nontoxic reaction products. It would be another advance in the art to provide a gas generating composition which produces very limited amounts of toxic or irritating particulate debris and limited undesirable gaseous products. It would also be an advance to provide a gas generating composition which forms a readily filterable slag upon reaction.
Such compositions and methods for their use are disclosed and claimed herein.
SUMMARY AND OBJECTS OF THE INVENTION
The present invention relates to a novel gas generating composition which is based on borohydride fuels and inorganic oxidizing agents which produce water vapor as the primary gaseous reaction product. The present composition comprises a mixture of finely divided borohydride fuel and an oxidizing agent containing oxygen and a metal comprising at least one member from the group consisting of a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, and mixtures thereof, provided that the borohydride fuel and the oxidizing agent are selected such that water vapor is produced when the composition is combusted.
The combustion reaction involves an oxidation-reduction reaction between the fuel and oxidizing agent. Under the exothermic conditions produced by the reaction, hydrogen from the borohydride reacts with oxygen from the oxidizing agent to produce water vapor and any water precursors in the oxidizing agent are also converted to water vapor. The water vapor is then available for use in deploying supplemental safety restraint devices such as inflating automobile air bags and the like.
It will be appreciated from the foregoing that the compositions of the present invention can generate large quantities of gas while avoiding some of the significant problems identified in the existing art. The gas generating compositions of the present invention are based on starting materials that produce substantially nontoxic reaction products.
These compositions produce only limited, if any, undesirable gaseous products. In addition, upon reaction, the gas generating compositions of the present invention produce only a limited amount, if any, of toxic or irritating debris while yielding a filterable slag.
These compositions combust rapidly and reproducibly to generate the substantially nontoxic gaseous reaction products described above.





DETAILED DESCRIPTION OF THE INVENTION
The compositions of the present invention include a borohydride fuel, in a fuel-effective amount and an oxidizing agent containing a metal and oxygen, in an oxidizer-effective amount. The fuel and the oxidizing agent combination is selected with the proviso that water vapor is the major gaseous product produced upon reaction between the fuel and the oxidizing agent and that essentially no, if any, hazardous gaseous reaction products are produced by that reaction. The fuel and the oxidizer are selected so that the combination of oxidizer and borohydride fuel exhibits reasonable thermal compatibility and chemical stability, that is, the combination of fuel and oxidizer does not begin reacting below about 225.degree. F. The borohydride fuel, oxidizer, or the combustion products therefrom, are preferably not highly toxic.
In the operation of a supplemental restraint device or related safety device according to the present invention, other gases, if any, are produced in concentrations that are low relative to the desired gaseous combustion product, water vapor.
The oxidizable borohydride fuel is selected from known and novel borohydrides, including, for example BH.sub.4.sup.-, B.sub.3 H.sub.8.sup.-, B.sub.8 H.sub.8.sup.2- B.sub.9 H.sub.15, B.sub.10.sub.14, B.sub.10 H.sub.10.sup.2-, B.sub.11 H.sub.14.sup.-, B.sub.12 H.sub.12.sup.2-, etc. and salts, complexes, and mixtures thereof. Currently preferred borohydride fuels include compounds based on BH.sub.4.sup.-, such as LiBH.sub.4, NaBH.sub.4, KBH.sub.4, RbBH.sub.4, CsBH.sub.4, Mg(BH.sub.4).sub.2, Ca(BH.sub.4).sub.2, Ba(BH.sub.4).sub.2, Al(BH.sub.4).sub.3, Zn(BH.sub.4).sub.3, and transition metal complexes of BH.sub.4.sup.-. Other preferred borohydride fuels are based on B.sub.12 H.sub.12.sup.2-, such as Li.sub.2 B.sub.12 H.sub.12, K.sub.2 B.sub.12 H.sub.12, Cs.sub.2 B.sub.12 H.sub.12, and [(CH.sub.3).sub.4 N].sub.2 B.sub.12 H.sub.12.
Both the oxidizable borohydride fuel and the oxidizer are incorporated into the composition in the form of a finely divided powder. Particle sizes typically range from about 0.001 .mu. to about 400 .mu., although the particle sizes preferably range from about 0.1 .mu. to about 50 .mu.. The composition is insertable into a gas generating device, such as a conventional supplemental safety restraint system, in the form of pellets or tablets. Alternatively, the composition is insertable in such devices in the form of a multi-perforated, high surface area grain or other solid form which allows rapid and reproducible generation of gas upon ignition.
An oxidizing agent containing a metal and oxygen is paired with the borohydride fuel. In the present context, an oxidizing agent used herein has the following characteristics:
(a) It is a compound or solid state phase containing at least one type of metal and oxygen.
(b) One or more of the metals contained therein can act as an oxidizing agent for the borohydride fuel found in the gas generant formulation.
Given the foregoing, the class of suitable inorganic oxidizers possessing the desired traits includes a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, or mixtures thereof wherein the metal species therein can be at least one species selected from elements from among Groups 5, 6, 7, 8, 9, 10, 11, 12, 14 and 15 as listed in the Periodic Table of the Elements according to the IUPAC format (CRC Handbook of Chemistry and Physics, (72nd Ed. 1991)). Examples of metal oxides include, among others, CuO, Co.sub.2 O.sub.3, Co.sub.3 O.sub.4, Bi.sub.2 O.sub.3, Fe.sub.2 O.sub.3, and CoFe.sub.2 O.sub.4. Examples of metal hydroxides include, among others, Fe(OH).sub.3, Co(OH).sub.3, Co(OH).sub.2, Ni(OH).sub.2, Cu(OH).sub.2, and Zn(OH).sub.2. Examples of metal oxide hydrates and metal hydrous oxides include, among others, Fe.sub.2 O.sub.3.xH.sub.2 O, SnO.sub.2.xH.sub.2 O, and MoO.sub.3.H.sub.2 O. Examples of metal oxide hydroxides include, among others, MnO(OH), MnO(OH).sub.2, FeO(OH), and MnO(OH).sub.3. In certain instances it will also be desirable to use mixtures of such oxidizing agents in order to enhance ballistic properties or maximize filterability of the slag formed from combustion of the composition. A preferred oxidizing agent is CuO.
In some cases, supplemental oxidizers such as alkali, alkaline earth, or ammonium perchlorates, chlorates, and peroxides in amounts up to about 40% by weight may be combined with the inorganic oxidizer to completely oxidize the fuel or enhance the burn rate.
The gas generant compositions of the present invention comprise a fuel-effective amount of borohydride fuel and an oxidizer-effective amount of at least one oxidizing agent. The present composition, in general, contains about 5 wt. % to about 40 wt. % borohydride fuel and from about 60 wt. % to about 95 wt. % oxidizing agent, and preferably from about 10 wt. % to about 30 wt. % fuel and from about 65 wt. % to about 90 wt. % oxidizing agent. These weight percentages are such that at least one oxidizing agent is present in an amount from about 0.5 to about 3 times the stoichiometric amount necessary to completely oxidize the borohydride fuel present.
Small quantities of other additives may also be included within the compositions if desired. Such additives are well known in the explosive, propellant, and gas generant arts. Such materials are conventionally added in order to modify the characteristics of the gas generating composition. Such materials include ballistic or burn rate modifiers, ignition aids, coolants, release agents or dry lubricants, binders for granulation or pellet crush strength, slag enhancers, anti-caking agents, etc. An additive often serves multiple functions. The additives may also produce gaseous reaction products to aid in the overall gas generation of the gas generant composition.
Ignition aids/burn rate modifiers include metal oxides, nitrates and other compounds such as, for instance, Fe.sub.2 O.sub.3, K.sub.2 B.sub.12.H.sub.12.H.sub.2 O, BiO(NO.sub.3), Co.sub.2 O.sub.3, CoFe.sub.2 O.sub.4, CuMoO.sub.4, Bi.sub.2 MoO.sub.6, MnO.sub.2, Mg(NO.sub.3).sub.2, Fe(NO.sub.3).sub.3, Co(NO.sub.3).sub.2, and NH.sub.4 NO.sub.3. Coolants include magnesium hydroxide, cupric oxalate, boric acid, aluminum hydroxide, and silicotungstic acid. Coolants such as aluminum hydroxide and silicotungstic acid can also function as slag enhancers. Small amounts of polymeric binders, such as polyethylene glycol or polypropylene carbonate can, if desired, be added for mechanical properties reasons or to provide enhanced crush strength. Examples of dry lubricants include MoS.sub.2, graphite, graphitic-boron nitride, calcium stearate and powdered polyethylene glycol (Avg. MW8000). The solid combustion products of most of the additives mentioned above will also enhance the filterability of the slag produced upon combustion of a gas generant formulation.
Illustrative examples of reactions involving compositions within the scope of the present invention are set forth in Table 1.
TABLE 1______________________________________ KBH.sub.4 + 2CuO + 1/2KClO.sub.4 .fwdarw. 2CU + 1/2KCl + KBO.sub.2 +2H.sub.2 O KBH.sub.4 + 2Cu(OH).sub.2 + 1/2KClO.sub.4 .fwdarw.2CU + KBO.sub.2 + 1/2KCl + 4H.sub.2 O3KBH.sub.4 + 2Bi.sub.2 O.sub.3 + 11/2KClO.sub.4 .fwdarw.4Bi + 3KBO.sub.2 + 11/2KCl + 6H.sub.2 O______________________________________
Computer modeling was performed for gas generant systems based on the reaction of Bi.sub.2 O.sub.3 oxidizer, KBH.sub.4 or NaBH.sub.4 fuel, and KClO.sub.4 supplemental oxidizer. The results are set forth below in Table 2.
TABLE 2__________________________________________________________________________Ingredient Weight Percent__________________________________________________________________________Bi.sub.2 O.sub.3 90 92 94 80 70 60 60 70 70NaBH.sub.4 10 8 6 10 10 10 -- -- --KClO.sub.4 -- -- -- 10 20 30 30 20 15KBH.sub.4 -- -- -- -- -- -- 10 10 15T (.degree.K.) 1828 1819 1805 2026 2197 2147 1768 1773 1984TP 0.77 0.67 0.55 0.66 0.58 0.62 0.64 0.59 0.58__________________________________________________________________________
Where T is the flame temperature and TP is the theoretical performance relative to a typical sodium azide based gas generant. Theoretical performance (gas volume and quantity) for a composition according to the present invention is comparable to those achieved by a conventional sodium azide-based gas generant composition. The theoretical performance for a typical sodium azide-based gas generant (68 wt. % NAN.sub.3 ; 30 wt. % of MoS.sub.2 ; 2 wt. % of S) is arbitrarily set equal to 1.0 and is about 0.85 g gas/cc NaN.sub.3 generant.
Computer modeling was performed for gas generant systems based on the reaction of Cu(OH).sub.2 oxidizer, KBH.sub.4 fuel, and KClO.sub.4 supplemental oxidizer. The results are set forth below in Table 3.
TABLE 3__________________________________________________________________________Ingredient Weight Percent__________________________________________________________________________Cu (OH).sub.2 90 85 80 80 75 70KBH.sub.4 10 15 20 10 15 20KClO.sub.4 -- -- -- 10 10 10T (.degree.K.) 1035 1227 1305 1389 1534 1549TP 1.06 1.01 1.01 0.89 0.92 0.93__________________________________________________________________________Ingredient Weight Percent__________________________________________________________________________Cu (OH).sub.2 70 65 60 60 55 50KBH.sub.4 10 15 20 10 15 20KClO.sub.4 20 20 20 30 30 30T (.degree.K.) 1504 1648 1664 1540 1814 2394TP 0.86 0.84 0.88 0.82 0.78 0.69__________________________________________________________________________
Computer modeling was performed for gas generant systems based on the reaction of CuO oxidizer, KBH.sub.4 fuel, and KClO.sub.4 supplemental oxidizer. The results are set forth below in Table 4.
TABLE 4__________________________________________________________________________Ingredient Weight Percent__________________________________________________________________________CuO 90 85 80 75 85 80 75 70KBH.sub.4 5 10 15 20 5 10 15 20KClO.sub.4 5 5 5 5 10 10 20 10T (.degree.K.) 1381 1555 1710 1680 1512 1613 1766 1740TP 0.23 0.39 0.55 0.65 0.23 0.40 0.54 0.64__________________________________________________________________________Ingredient Weight Percent__________________________________________________________________________CuO 80 75 70 65 75 70 65 60KBH.sub.4 5 10 15 20 5 10 15 20KClO.sub.4 15 15 15 15 20 20 20 20T (.degree.K.) 1560 1618 1873 1899 1571 1622 1989 2073TP 0.26 0.45 0.52 0.63 0.32 0.49 0.50 0.60__________________________________________________________________________
The theoretical flame temperatures of the reaction between the fuel and the oxidizing agent are in the range of from about 1000.degree. K. to about 2200.degree. K., with the more preferred range being from about 1500.degree. K. to about 1800.degree. K. This is a manageable range for application in the field of automobile air bags and can be adjusted to form non-liquid (e.g., solid) easily filterable slag.
With the reaction characteristics, the compositions and methods of the present invention can produce a sufficient volume and quantity of gas to inflate a supplemental safety restraint device, such as an automobile air bag, at a manageable temperature. The reaction of the compositions within the scope of the invention produce significant quantities of water vapor in a very short period of time. At the same time, the reaction substantially avoids the production of unwanted gases and particulate materials, although minor amounts of other gases may be produced. The igniter formulation may also produce small amounts of other gases.
The present gas generant compositions can be formulated to produce an integral slag to limit substantially the particulate material produced. This minimizes the production of solid particulate debris outside the combustion chamber. Thus, it is possible to substantially avoid the production of a caustic powder, such as sodium oxide/hydroxide or sodium sulfide, commonly produced by conventional sodium azide formulations.
The compositions of the present invention are ignited with conventional igniters. Igniters using materials such as boron/potassium nitrate are usable with the compositions of the present invention. Thus, it is possible to substitute the compositions of the present invention in state-of-the-art gas generant applications.
The gas generating compositions of the present invention are readily adapted for use with conventional hybrid air bag inflator technology. Hybrid inflator technology is based on heating a stored inert gas (argon or helium) to a desired temperature by burning a small amount of propellant. Hybrid inflators do not require cooling filters used with pyrotechnic inflators to cool combustion gases, because hybrid inflators are able to provide a lower temperature gas. The gas discharge temperature can be selectively changed by adjusting the ratio of inert gas weight to propellant weight. The higher the gas weight to propellant weight ratio, the cooler the gas discharge temperature.
A hybrid gas generating system comprises a pressure tank having a rupturable opening, a pre-determined amount of inert gas disposed within that pressure tank; a gas generating device for producing hot combustion gases and having means for rupturing the rupturable opening; and means for igniting the gas generating composition. The tank has a rupturable opening which can be broken by a piston when the gas generating device is ignited. The gas generating device is configured and positioned relative to the pressure tank so that hot combustion gases are mixed with and heat the inert gas. Suitable inert gases include, among others, argon, and helium and mixtures thereof. The mixed and heated gases exit the pressure tank through the opening and ultimately exit the hybrid inflator and deploy an inflatable bag or balloon, such as an automobile air bag. The gas generating device contains a gas generating composition according to the present invention which comprises an oxidizable borohydride fuel and an oxidizing agent selected from basic metal carbonates and basic metal nitrates. The oxidizable borohydride fuel and oxidizing agent being selected so that substantially nontoxic gases are produced such as mixtures of water vapor and either carbon dioxide or nitrogen.
The high heat capacity of water vapor produced is an added advantage for its use as a heating gas in a hybrid gas generating system. Thus, less water vapor, and consequently, less generant is needed to heat a given quantity of inert gas to a given temperature.
Hybrid gas generating devices for supplemental safety restraint application are described in Frantom, Hybrid Airbag Inflator Technology, Airbag Int'l Symposium on Sophisticated Car Occupant Safety Systems, (Weinbrenner-Saal, Germany, Nov. 2-3, 1992).
An automobile air bag system can comprise a collapsed, inflatable air bag, a gas generating device connected to the air bag for inflating the air bag, and means for igniting the gas generating composition. The gas generating device contains a gas generating composition comprising an oxidizable borohydride fuel and an oxidizing agent, wherein said oxidizing agent comprises at least one member selected from the group consisting of a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, or mixtures thereof, and wherein water vapor is the major gaseous reaction product generated by reaction between said oxidizable borohydride fuel and said oxidizing agent.
EXAMPLES
The present invention is further described in the following nonlimiting examples. Unless otherwise stated, the compositions are expressed in weight percent.
Example 1
A gas generant composed of 85.5% CuO, 10.0% NaBH.sub.4, and 5.0% KClO.sub.4 was mixed in hexane at low shear. The hexane was removed under vacuum. The powder was pressed into 0.25 inch by 0.5 inch diameter pellets which exhibit a burning rate of 0.84 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.60 with a combustion temperature of 1915.degree. K. The major combustion products were 43.5 mole % liquid Cu, 30.2 mole % H.sub.2 O, 15.2 mole % borates, 8.9 mole % liquid Cu.sub.2 O, and 1.54 mole % KCl and NaCl.
Example 2
A gas generant composed of 70.0% CuO, 10.0% NaBH.sub.4, and 20.0% KClO.sub.4 was mixed in hexane at low shear. The hexane was removed under vacuum. The powder was pressed into 0.25 inch by 0.5 inch diameter pellets which exhibit a burning rate of 1.21 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.52 with a combustion temperature of 2015.degree. K. The major combustion products were 37.1 mole % H.sub.2 O, 28.5 mole % Cu.sub.2 O, 18.7 mole % borates, 5.6 mole % liquid Cu, and 6.0 mole % KCl and NaCl.
Example 3
A gas generant composed of 75% CuO, 15.0% NaBH.sub.4, and 10.0% KClO.sub.4 was mixed in hexane at low shear. The hexane was removed under vacuum. The powder was pressed into 0.25 inch by 0.5 inch diameter pellets which exhibit a burning rate of 1.27 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.54 with a combustion temperature of 1766.degree. K. The major combustion products were 41.2 mole % liquid Cu, 32.0 mole % H.sub.2 O, 14.7 mole % borates, 7 mole % liquid Cu.sub.2 O, and 4.0 mole % KCl.
Example 4
A gas generant composed of 55.0% Cu(OH).sub.2, 15.0% KBH.sub.4, and 30% KClO.sub.4 was mixed in hexane under low shear. The hexane was removed under vacuum at ambient temperature. The powdered generant was pressed into 0.5 inch pellets which exhibit a burning rate of 0.48 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.78 with a combustion temperature of 1814.degree. K. The major combustion products were 58.5 mole % H.sub.2 O, 14.9 mole % liquid Cu.sub.2 O, 14.1 mole % KBO.sub.2, 8.83 mole % liquid KCl, and 1.63 mole % KCl vapor.
Example 5
A gas generant composed of 65.0% Cu(OH).sub.2, 15.0% KBH.sub.4, and 20% KClO.sub.4 was mixed in hexane under low shear. The hexane was removed under vacuum at ambient temperature. The powdered generant was pressed into 0.5 inch pellets which exhibit a burning rate of 0.55 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.85 with a combustion temperature of 1648.degree. K. The major combustion products were 56.3 mole % H.sub.2 O, 18.9 mole % liquid Cu, 9.0 mole % KBO.sub.2, 6.2 mole % liquid Cu.sub.2 O, 1.0 mole % liquid K.sub.2 B.sub.4 O.sub.7, and 6.0 mole % KCl.
Example 6
A gas generant composed of 64% Cu(OH).sub.2, 1% Fe.sub.2 O.sub.3, 15% KBH.sub.4, and 20% KClO.sub.4 was mixed in hexane at low shear. The hexane was removed under vacuum at ambient temperature. The powdered generant was pressed into 0.5 inch pellets which exhibit a burning rate of 0.28 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.84 with a combustion temperature of 1649.degree. K. The major combustion products were 56 mole % H.sub.2 O, 19.2 mole % liquid Cu, 9.2 mole % KBO.sub.2, 5.8 mole % liquid Cu.sub.2 O, 1.0 mole % liquid K.sub.2 B.sub.4 O.sub.7, 1.4% KOH, and 6.0 mole % liquid KCl.
Example 7
A gas generant composed of 63.5% Cu(OH).sub.2, 15.0% KBH.sub.4, 1.5% Li.sub.2 B.sub.12 H.sub.12, and 20% KClO.sub.4 was mixed in hexane at low shear. The hexane was removed under vacuum at ambient temperature. The powdered generant was pressed into 0.5 inch pellets which exhibit a burning rate of 0.72 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.86 with a combustion temperature of 1876.degree. K. The major combustion products were 48.7 mole % H.sub.2 O, 28.1 mole % liquid Cu, 8.9 mole % KBO.sub.2, 5.4 mole % H.sub.2, 1.7 mole % liquid K.sub.2 B.sub.4 O.sub.7, 2.9 mole % liquid KCl, and 2.0 mole % KCl vapor.
Example 8
A gas generant composed of 63.5% Cu(OH).sub.2, 15.0% KBH.sub.4, 1.5% ((CH.sub.3).sub.4 N).sub.2 B.sub.12 H.sub.12, and 20% KClO.sub.4 was mixed in hexane at low shear. The hexane was removed under vacuum at ambient temperature. The powdered generant was pressed into 0.5 inch pellets which exhibit a burning rate of 0.53 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.90 with a combustion temperature of 1842.degree. K. The major combustion products were 49.4 mole % H.sub.2 O, 27.7 mole liquid Cu, 8.6 mole % KBO.sub.2, 5.4 mole % H.sub.2, 1.6 mole % liquid K.sub.2 B.sub.4 O.sub.7, 3.5 mole % liquid KCl, and 1.7 mole % KCl vapor.
Example 9
A gas generant composed of 70% Bi.sub.2 O.sub.3, 10% NaBH.sub.4, and 20% KClO.sub.4 was mixed in hexane at low shear. The hexane was removed under vacuum at ambient temperature. The powdered generant was pressed into 0.5 inch pellets which exhibited a burning rate of 2.3 ips at 1000 psi. Based on computer modeling, the theoretical performance of this composition was 0.58 with a combustion temperature of 2197.degree. K. The major combustion products were 39.8 mole % H.sub.2 O, 20.1 mole % liquid Bi, 7.0 mole % KBO.sub.2, 5.7 mole % NaCl,4.4 mole % Bi vapor, 3.9 mole % KCl, and 2.3 mole % H.sub.2.
Example 10
Theoretical calculations were conducted on the reaction of KBH.sub.4, Bi.sub.2 O.sub.3, and KClO.sub.4, as listed in Table 1, to evaluate its use in a hybrid gas generator. If this formulation is allowed to undergo combustion in the presence of 1.5 times its weight argon gas, the flame temperature decreases from 2123.degree. K. to 1440.degree. K., assuming 100% efficient heat transfer. The output gases consist of 87% by volume argon and 10% by volume water vapor.
From the foregoing, it will be appreciated that the present invention provides compositions capable of generating large quantities of gas which are based on substantially nontoxic starting materials and which produce substantially nontoxic reaction products. The gas generant compositions of the present invention also produce very limited amounts of toxic or irritating particulate debris and limited undesirable gaseous products. In addition, the present invention provides gas generating compositions which form a readily filterable solid slag upon reaction.
The invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is, therefore, indicated by the appended claims rather than by the foregoing description. All changes which come within the meaning and range of equivalency of the claims are to be embraced within their scope.
Claims
  • 1. A solid gas-generating composition comprising an oxidizable borohydride fuel and an oxidizing agent, wherein said oxidizing agent comprises at least one member selected from the group consisting of a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, or mixtures thereof, and wherein water vapor is the major gaseous reaction product generated by reaction between said oxidizable borohydride fuel and said oxidizing agent.
  • 2. A solid gas-generating composition according to claim 1, comprising from about 5 wt. % to about 40 wt. % borohydride fuel and from about 95 wt. % to about 60 wt. % oxidizing agent.
  • 3. A solid gas-generating composition according to claim 1, wherein the oxidizable borohydride fuel is selected from salts or complexes of BH.sub.4.sup.-, B.sub.3 H.sub.8.sup.-, B.sub.8 H.sub.8.sup.2-, B.sub.9 H.sub.15, B.sub.10 H.sub.14, B.sub.10 H.sub.10.sup.2-, B.sub.11 H.sub.14.sup.-, B.sub.12 H.sub.12.sup.2-, and mixtures thereof.
  • 4. A solid gas-generating composition according to claim 1, wherein the oxidizable borohydride fuel is based on BH.sub.4.sup.-.
  • 5. A solid gas-generating composition according to claim 4, wherein the oxidizable borohydride fuel is selected from LiBH.sub.4, NaBH.sub.4, KBH.sub.4, RbBH.sub.4, CsBH.sub.4, Mg(BH.sub.4).sub.2, Ca(BH.sub.4).sub.2, Ba(BH.sub.4).sub.2, Al(BH.sub.4).sub.3, Zn(BH.sub.4).sub.3, transition metal complexes of BH.sub.4.sup.-, and mixtures thereof.
  • 6. A solid gas-generating composition according to claim 1, wherein the oxidizable borohydride fuel and the oxidizer are in the form of a finely divided powder.
  • 7. A solid gas-generating composition according to claim 6, wherein the particle size range of the powder is from about 0,001 .mu. to about 400 .mu..
  • 8. A solid gas-generating composition according to claim 1, wherein the oxidizing agent is a metal oxide selected from CuO, Co.sub.2 O.sub.3, Co.sub.3 O.sub.4, Bi.sub.2 O.sub.3, Fe.sub.2 O.sub.3, CoFe.sub.2 O.sub.4, and mixtures thereof.
  • 9. A solid gas-generating composition according to claim 1, wherein the oxidizing agent is a metal hydroxide selected from Fe(OH).sub.3, Co(OH).sub.3, Co(OH).sub.2, Ni(OH).sub.2, Cu(OH).sub.2, Zn(OH).sub.2, and mixtures thereof.
  • 10. A solid gas-generating composition according to claim 1, wherein the oxidizing agent is a hydrated metal oxide selected from Fe.sub.2 O.sub.3.xH.sub.2 O, SnO.sub.2.xH.sub.2 O, MoO.sub.3.H.sub.2 O, and mixtures thereof.
  • 11. A solid gas-generating composition according to claim 1, wherein the oxidizing agent is a metal oxide hydroxide selected from MnO(OH), MnO(OH).sub.2, FeO(OH), MnO(OH).sub.3, and mixtures thereof.
  • 12. An automobile air bag system comprising:
  • a collapsed, inflatable air bag;
  • a gas-generating device connected to the air bag for inflating said air bag, said gas-generating device containing a gas-generating composition comprising an oxidizable borohydride fuel and an oxidizing agent, wherein said oxidizing agent comprises at least one member selected from the group consisting of a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, or mixtures thereof, and wherein water vapor is the major gaseous product generated by said solid gas-generating composition; wherein said oxidizing agent is present in an amount from about 0.5 to about 3 times the stoichiometric amount of oxidizing agent necessary to completely oxidize the borohydride present; and
  • means for igniting said gas-generating composition.
  • 13. An automobile air bag system according to claim 12, wherein said gas-generating composition comprises from about 5 wt. % to about 40 wt. % oxidizable borohydride fuel and from about 95 wt. % to about 60 wt. % oxidizing agent.
  • 14. An automobile air bag system according to claim 12, wherein the oxidizable borohydride fuel is selected from BH.sub.4.sup.-, B.sub.3 H.sub.8.sup.-, B.sub.8 H.sub.8.sup.2-, B.sub.9 H.sub.15, B.sub.10 H.sub.14, B.sub.10 H.sub.10.sup.2-, B.sub.11 H.sub.14.sup.-, B.sub.12 H.sub.12.sup.2-, and mixtures thereof.
  • 15. An automobile air bag system according to claim 12, wherein the oxidizable borohydride fuel is based on BH.sub.4.sup.-.
  • 16. An automobile air bag system according to claim 15, wherein the oxidizable borohydride fuel is selected from LiBH.sub.4, NaBH.sub.4, KBH.sub.4, RbBH.sub.4, CsBH.sub.4, Mg(BH.sub.4).sub.2, Ca(BH.sub.4).sub.2, Ba(BH.sub.4).sub.2, Al(BH.sub.4).sub.3, Zn(BH.sub.4).sub.3, transition metal complexes of BH.sub.4.sup.-, and mixtures thereof.
  • 17. An automobile air bag system according to claim 12, wherein the oxidizing agent is a metal oxide selected from CuO, Co.sub.2 O.sub.3, Co.sub.3 O.sub.4, Bi.sub.2 O.sub.3, Fe.sub.2 O.sub.3, CoFe.sub.2 O.sub.4, and mixtures thereof.
  • 18. An automobile air bag system according to claim 12, wherein the oxidizing agent is a metal hydroxide selected from Fe(OH).sub.3, Co(OH).sub.3, Co(OH).sub.2, Ni(OH).sub.2, Cu(OH).sub.2, Zn(OH).sub.2, and mixtures thereof.
  • 19. An automobile air bag system according to claim 12, wherein the oxidizing agent is a hydrated metal oxide selected from Fe.sub.2 O.sub.3. xH.sub.2 O, SnO.sub.2.xH.sub.2 O, MoO.sub.3 H.sub.2 O, and mixtures thereof.
  • 20. An automobile air bag system according to claim 12, wherein the oxidizing agent is a metal oxide hydroxide selected from MnO(OH), MnO(OH).sub.2, FeO(OH), MnO(OH).sub.3, and mixtures thereof.
  • 21. An automobile air bag system having a hybrid gas-generating system comprising:
  • a collapsed, inflatable air bag;
  • a pressure tank having a rupturable opening, said pressure tank containing an inert gas;
  • a gas-generating device for producing hot combustion gases and capable of rupturing the rupturable opening, said gas-generating device being configured in relation to the pressure tank such that hot combustion gases are mixed with and heat the inert gas and wherein said gas-generating device and the pressure tank are connected to the inflatable air bag such that the combustion gases and inert gas are capable of inflating the air bag, said gas-generating device containing a gas-generating composition comprising an oxidizable borohydride fuel and an oxidizing agent, wherein said oxidizing agent comprises at least one member selected from the group consisting of a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, or mixtures thereof, and wherein water vapor is the major gaseous product generated by said solid gas-generating composition; wherein said oxidizing agent is present in an amount from about 0.5 to about 3 times the stoichiometric amount of oxidizing agent necessary to completely oxidize the borohydride present; and
  • means for igniting the gas-generating composition.
  • 22. An automobile air bag system according to claim 21, wherein said inert gas is argon or helium.
  • 23. An automobile air bag system according to claim 21, wherein said gas-generating composition comprises from about 5% to about 40% borohydride fuel and from about 95% to about 60% oxidizing agent.
  • 24. An automobile air bag system according to claim 21, wherein the oxidizable borohydride fuel is selected from BH.sub.4.sup.-, B.sub.3 H.sub.8.sup.-, B.sub.8 H.sub.8.sup.2-, B.sub.9 H.sub.15, B.sub.10 H.sub.14, B.sub.10 H.sub.10.sup.2-, B.sub.11 H.sub.14.sup.-, B.sub.12 H.sub.12.sup.2-, and mixtures thereof.
  • 25. An automobile air bag system according to claim 21, wherein the oxidizable borohydride fuel is based on BH.sub.4.sup.-.
  • 26. An automobile air bag system according to claim 25, wherein the oxidizable borohydride fuel is selected from LiBH.sub.4, NaBH.sub.4, KBH.sub.4, RbBH.sub.4, CsBH.sub.4, Mg(BH.sub.4).sub.2, Ca(BH.sub.4).sub.2, Ba(BH.sub.4).sub.2, Al(BH.sub.4).sub.3, Zn(BH.sub.4).sub.3, transition metal complexes of BH.sub.4.sup.-, and mixtures thereof.
  • 27. An automobile air bag system according to claim 21, wherein the oxidizing agent is a metal oxide selected from CuO, Co.sub.2 O.sub.3, Co.sub.3 O.sub.4, Bi.sub.2 O.sub.3, Fe.sub.2 O.sub.3, CoFe.sub.2 O.sub.4, and mixtures thereof.
  • 28. An automobile air bag system according to claim 21, wherein the oxidizing agent is a metal hydroxide selected from Fe(OH).sub.3, Co(OH).sub.3, Co(OH).sub.2, Ni(OH).sub.2, Cu(OH).sub.2, Zn(OH).sub.2, and mixtures thereof.
  • 29. An automobile air bag system according to claim 21, wherein the oxidizing agent is a hydrated metal oxide selected from Fe.sub.2 O.sub.3.xH.sub.2 O, SnO.sub.2.xH.sub.2 O, MoO.sub.3.H.sub.2 O, and mixtures thereof.
  • 30. An automobile air bag system according to claim 21, wherein the oxidizing agent is a metal oxide hydroxide selected from MnO(OH).sub.2, MnO(OH).sub.2, FeO(OH), MnO(OH).sub.3, and mixtures thereof.
  • 31. A vehicle containing a supplemental restraint system having an air bag system comprising:
  • a collapsed, inflatable air bag,
  • a gas-generating device connected to said air bag for inflating said air bag, said gas-generating device containing a gas-generating composition comprising an oxidizable borohydride fuel and an oxidizing agent, wherein said oxidizing agent comprises at least one member selected from the group consisting of a metal oxide, a metal oxide hydrate, a metal oxide hydroxide, a metal hydrous oxide, a metal hydroxide, or mixtures thereof, and wherein water vapor is the major gaseous product generated by said solid gas-generating composition; wherein said oxidizing agent is present in an amount from about 0.5 to about 3 times the stoichiometric amount of oxidizing agent necessary to completely oxidize the borohydride present; and
  • means for igniting said gas-generating composition.
  • 32. A vehicle as defined in claim 31, further comprising a pressure tank having a rupturable opening, said pressure tank containing an inert gas; wherein the gas-generating device produces hot combustion gases capable of rupturing the rupturable opening, and wherein the gas-generating device is configured in relation to the pressure tank such that hot combustion gases are mixed with and heat the inert gas and wherein the gas-generating device and the pressure tank are connected to the inflatable air bag such that the mixture of combustion gases and inert gas are capable of inflating the air bag.
RELATED APPLICATION

This invention is a continuation-in-part of copending U.S. patent application Ser. No. 08/103,768, filed Aug. 10, 1993, titled "Thermite Compositions for Use as Gas Generants," which is incorporated herein by reference.

US Referenced Citations (135)
Number Name Date Kind
H464 Lee et al. May 1988
147871 Shaw Feb 1874
2483803 Bridgman et al. Oct 1949
2981616 Boyer Apr 1961
3010815 Pierce et al. Nov 1961
3122462 Kaufman et al. Feb 1964
3405068 Hiltz Oct 1968
3447955 Hiltz Nov 1969
3450414 Kobori Jun 1969
3674059 Stephenson Jul 1972
3711115 Lohr Jan 1973
3723205 Scheffee Mar 1973
3773351 Catanzarite Nov 1973
3773352 Radke Nov 1973
3773947 Boyars et al. Nov 1973
3775182 Marshall Aug 1973
3779823 Price et al. Dec 1973
3785149 Timmerman Jan 1974
3787074 Lewis et al. Jan 1974
3791302 McLeod Feb 1974
3806461 Hendrickson et al. Apr 1974
3810655 Pracher May 1974
3814694 Klager Jun 1974
3827715 Lynch Aug 1974
3833029 Munn Sep 1974
3833432 Moy et al. Sep 1974
3837942 Catanzarite Sep 1974
3862866 Timmerman et al. Jan 1975
3868124 Johnson Feb 1975
3880447 Thorn et al. Apr 1975
3880595 Timmerman Apr 1975
3883373 Sidebottom May 1975
3895098 Pietz Jul 1975
3897285 Hamilton et al. Jul 1975
3901747 Garner Aug 1975
3902934 Timmerman Sep 1975
3910805 Catanzarite Oct 1975
3912458 Fukuma et al. Oct 1975
3912561 Doin et al. Oct 1975
3912562 Garner Oct 1975
3931040 Breazeale Jan 1976
3933543 Madden Jan 1976
3934984 Marlow et al. Jan 1976
3936330 Dergazarian et al. Feb 1976
3947300 Passauer et al. Mar 1976
3948699 Ayers Apr 1976
3950009 Hamilton Apr 1976
3964255 Catanzarite Jun 1976
3971729 Timmerman Jul 1976
3996079 Divalentin Dec 1976
4021275 Kishi et al. May 1977
4062708 Goetz Dec 1977
4114591 Nakagawa Sep 1978
4124515 Gruner et al. Nov 1978
4128996 Garner et al. Dec 1978
4141734 Misra Aug 1992
4152891 Garner May 1979
4157648 Brennan et al. Jun 1979
4179327 Seldner Dec 1979
4200615 Hamilton et al. Apr 1980
4203786 Garner May 1980
4203787 Kirchoff et al. May 1980
4214438 Hamilton et al. Jul 1980
4238253 Garner Dec 1980
4244758 Garner et al. Jan 1981
4246051 Garner et al. Jan 1981
4298412 Biddle et al. Nov 1981
4306499 Holmes Dec 1981
4339288 Camp Jul 1982
4369079 Shaw Jan 1983
4370181 Lundstrom et al. Jan 1983
4370930 Strasser et al. Feb 1983
4376002 Utracki Mar 1983
4390380 Camp Jun 1983
4407119 Biddle et al. Oct 1983
4414902 Strasser et al. Nov 1983
4424086 Christopher Jan 1984
4484960 Rucker Nov 1984
4533416 Poole Aug 1985
4547235 Schneiter et al. Oct 1985
4547342 Adams et al. Oct 1985
4578247 Bolieau Mar 1986
4590860 Kromrey May 1986
4604151 Knowlton et al. Aug 1986
4664033 Burkdoll et al. May 1987
4690063 Granier et al. Sep 1987
4696705 Hamilton Sep 1987
4698107 Goetz et al. Oct 1987
4699400 Adams et al. Oct 1987
4734141 Cartwright et al. Mar 1988
4758287 Pietz Jul 1988
4798142 Centerberry et al. Jan 1989
4806180 Goetz et al. Feb 1989
4833996 Hayashi et al. May 1989
4834817 Zeuner et al. May 1989
4834818 Kazumi et al. May 1989
4865667 Zeuner et al. Sep 1989
4890860 Schneiter Jan 1990
4909549 Poole et al. Mar 1990
4919897 Bender et al. Apr 1990
4931111 Poole et al. Jun 1990
4931112 Wardle et al. Jun 1990
4948439 Poole et al. Aug 1990
4950458 Cunningham Aug 1990
4959011 Nilsson Sep 1990
4963203 Halcomb et al. Oct 1990
4981534 Scheffe Jan 1991
4982664 Norton Jan 1991
4998751 Paxton et al. Mar 1991
5003887 Unterforsthuber et al. Apr 1991
5004586 Hayashi et al. Apr 1991
5005486 Lenzen Apr 1991
5015309 Wardle et al. May 1991
5015311 Ramaswamy May 1991
5019192 Ramaswamy May 1991
5019220 Taylor et al. May 1991
5022674 Frantom et al. Jun 1991
5024160 Canterberry et al. Jun 1991
5031932 Frantom et al. Jul 1991
5033390 Minert et al. Jul 1991
5043030 Ramaswamy Aug 1991
5046429 Swann et al. Sep 1991
5052817 Bement et al. Oct 1991
5060973 Giovanetti Oct 1991
5062365 Canterberry Nov 1991
5062367 Hayashi et al. Nov 1991
5073273 Gupta et al. Dec 1991
5074940 Ochi et al. Dec 1991
5089069 Ramaswamy et al. Feb 1992
5094475 Olsson et al. Mar 1992
5098597 Rothgery et al. Mar 1992
5100172 Vanvoorhies et al. Mar 1992
5100174 Jasken et al. Mar 1992
5104466 Allard et al. Apr 1992
5212343 Brupacher et al. May 1993
Continuation in Parts (1)
Number Date Country
Parent 103768 Aug 1993