EP1526121A1 - Gas generating composition - Google Patents

Gas generating composition Download PDF

Info

Publication number
EP1526121A1
EP1526121A1 EP04024216A EP04024216A EP1526121A1 EP 1526121 A1 EP1526121 A1 EP 1526121A1 EP 04024216 A EP04024216 A EP 04024216A EP 04024216 A EP04024216 A EP 04024216A EP 1526121 A1 EP1526121 A1 EP 1526121A1
Authority
EP
European Patent Office
Prior art keywords
gas generating
generating composition
composition
component
mass
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP04024216A
Other languages
German (de)
French (fr)
Other versions
EP1526121B1 (en
Inventor
Jianzhou Wu
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daicel Corp
Original Assignee
Daicel Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daicel Chemical Industries Ltd filed Critical Daicel Chemical Industries Ltd
Publication of EP1526121A1 publication Critical patent/EP1526121A1/en
Application granted granted Critical
Publication of EP1526121B1 publication Critical patent/EP1526121B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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

Definitions

  • the invention relates to a gas generating composition to be used for a gas generator for an air bag.
  • a gas generating composition comprises fuel, an oxidizing agent and a variety of additives to be added based on the necessity, and the composition is required to satisfy that the gas generated by combustion is clean, in other words, the gas contains no nitrogen oxide (NOx), CO, or the like.
  • NOx nitrogen oxide
  • BCN basic copper nitrate
  • a chloric acid compound also well-known as an oxidizing agent causes NOx removal reaction and becomes a supply source of oxygen required to decompose NOx into nitrogen and water, and therefore it has been used widely.
  • EP-B No. 1, 006, 096 and US-A1 No. 2003/0145921 BCN is used as an oxidizing agent to decrease the combustion temperature and accordingly the discharged gas is cleaned and a satisfactory burning rate is obtained.
  • the use ratio of the perchloric acid salt to BCN is high and the supply of oxygen becomes excess, so that, the generation amounts of NOx and mist are unsatisfactorily increased.
  • a purpose of the invention is to provide a gas generating composition with a good ignition property and combustibility and generating suppressed amounts of toxic gases such as NOx and ammonia at the time of combustion.
  • the invention provides a gas generating composition
  • a gas generating composition comprising (A) a nitrogen-containing compound as fuel and (B) a basic metal nitrate and (C) a chloric acid compound as oxidizing agents, the chloric acid compound (C) being selected from (C-1) a perchloric acid salt and (C-2) a chloric acid salt, the content of the component (C) being less than 5% by mass in the total oxidizing agents.
  • the composition of the invention has a good ignition property and combustibility (a high burning rate) and can decrease the generation amounts of NOx and ammonia gas at the time of combustion, so that the amounts of NOx and ammonia to be contained in the combustion gas can be suppressed.
  • composition of the invention is applied to a gas generator for an air bag, a necessary amount of a gas for expansion can be generated within a time to reliably protect a passenger and at the same time, the toxic gas amount can remarkably be suppressed in the gas for expanding the air bag and thus, the safety can be enhanced.
  • the fuel to be used in the invention contains a nitrogen-containing compound as the component (A), and as the nitrogen-containing compound, at least one selected from tetrazole compounds, guanidine compounds, triazine compounds and nitroamine compounds.
  • the nitrogen-containing compound other than the nitrogen-containing compound, known fuel may be contained and in such a case, the ratio of the nitrogen-containing compound in the fuel is preferably 20% or more by mass.
  • the tetrazoles 5-aminotetrazole and bitetrazole ammonium are preferable.
  • guanidine nitric acid salt nitric acid guanidine
  • aminoguanidine nitric acid salt aminoguanidine nitric acid salt
  • nitroguanidine and triaminoguanidine nitric acid salt
  • triazines melamine, cyanuric acid, ammeline, ammelide, and ammeland are preferable.
  • nitroamines cyclo-1,3,5-trimethine-2,4,6-trinitramine is preferable.
  • guanidine nitric acid salt is particularly preferable.
  • the content of the component (A) is preferably 15 to 50% by mass, more preferably 20 to 55% by mass, and even more preferably 25 to 50% by mass.
  • the oxidizing agent to be used in the invention includes the basic metal nitrate (B) , the chloric acid compound (C) , and additionally other oxidizing agents to be used based on the necessity.
  • An example of the basic metal nitrate of the component (B) can be at least one of the compounds selected from basic copper nitrate, basic cobalt nitrate, basic zinc nitrate, basic manganese nitrate, basic iron nitrate, basic molybdenum nitrate, basic bismuth nitrate, and basic cerium nitrate.
  • the basic metal nitrate is preferable to have the average particle diameter of 30 ⁇ m or smaller, more preferably 10 ⁇ m or smaller.
  • the average particle diameter is measured according to a particle size distribution method using laser scattered beam.
  • the measurement sample is prepared by dispersing the basic metal nitrate in water and radiating ultrasonic wave for 3 minutes, and 50% cumulative values (D 50 ) of the particles are calculated and the average of the values measured twice is employed as the average particle diameter.
  • the chloric acid compound of the component (C) is a component having an oxidizing function and a combustion promoting function.
  • the oxidizing function means to generate oxygen during the combustion and accordingly to efficiently promote combustion as well as to suppress the production amount of the toxic gases such as NOx, ammonia, carbon monoxide and the like.
  • the combustion promoting function means to improve the ignition property of the gas generating composition or to improve the burning rate (enhancing the combustibility).
  • the chloric acid compound of the component (C) may include the perchloric acid salt (C-1) and/or the chloric acid salt (C-2).
  • the perchloric acid salt of the component (C-1) may include ammonium perchlorate, potassium perchlorate, and sodium perchlorate.
  • the chloric acid salt of the component (C-2) may include chloric acid, potassium chlorate, and sodium chlorate, and among them, sodium perchlorate is particularly preferable.
  • the chloric acid compound of the component (C) is preferable to have the average particle diameter of 1 to 500 ⁇ m, more preferably 2 to 50 ⁇ m.
  • the measurement method of the average particle diameter is the same as that of the average particle diameter of the component (B).
  • the total content of the oxidizing agents of the component (B) and component (C) is preferably 30 to 70% by mass, more preferably 35 to 60% by mass, and even more preferably 40 to 55% by mass in the gas generating composition.
  • the content of the component (C) in the total oxidizing agent is less than 5% by mass, preferably 1 to 5% by mass, and even more preferably 2 to 5% by mass. If the content of the component (C) is less than 5% by mass, the combustion temperature can be lowered.
  • the mass ratio (B)/(C) of the basic copper nitrate (B) and the chloric acid compound (C) in the oxidizing agents is preferably in the range of 3 to 70, more preferably 3 to 25, furthermore preferably 5 to 25, still more preferably 7 to 20, and most preferably 5 to 20.
  • the ignition property of the composition is improved and the combustibility (the burning rate) is also improved and at the same time, the production amounts of NOx and ammonia are suppressed at the time of the combustion and therefore, the combustion gas is clean.
  • the content of the basic copper nitrate (B) in the total oxidizing agents is 50% by mass or more, preferably 60% by mass or more, and still preferably 70% by mass or more. If the content of component (B) is in the above range, the ignition property of the composition is improved and the combustibility (the burning rate) is also improved.
  • the composition of the invention may further contain the component (D) of a metal hydroxide, a hydrated metal oxide, or a combination thereof as a coolant.
  • the coolant has a function for lowering the combustion temperature.
  • the component (D) greatly absorbs heat when it is thermally decomposed and produced an oxide and water. Therefore, addition of the component (D) is effective to decrease the combustion temperature of the composition and suppress the production amounts of toxic NOx and carbon monoxide.
  • metal hydroxide of the component (D) can be magnesium hydroxide, aluminum hydroxide, calcium hydroxide, zirconium hydroxide, cobalt hydroxide and copper hydroxide, and an example of the hydrated metal oxide can be hydrated aluminum oxide.
  • the component (D) can improve the entire dispersibility when the components (A) to (C) are mixed, so that the mixing work is made easy and the ignition property of the obtained composition can be improved.
  • the average particle diameter of the component (D) is preferably 0.1 to 70 ⁇ m, more preferably 0.5 to 50 ⁇ m, and even more preferably 2 to 30 ⁇ m.
  • the measurement method of the average particle diameter is the same measurement method of the average particle diameter of the component (B).
  • the content of the component (D) in the gas generating composition is preferably 1 to 15% by mass, more preferably 3 to 12% by mass, and even more preferably 5 to 10% by mass.
  • the composition of the invention may contain a binder.
  • the binder is a component to be used together with the components (A) to (C) based on the necessity and is a component to improve the formability of the composition and increase the strength of a molded article of the gas generating agent. If the strength of a molded article of the gas generating agent is insufficient, it may occur that the molded article breaks at the time of actual combustion and is burned too intensely to control the combustion.
  • the binder may be at least one compound selected from carboxymethyl cellulose, carboxymethyl cellulose sodium salt, carboxymethyl cellulose potassium salt, carboxymethyl cellulose ammonium salt, cellulose acetate, cellulose acetate butyrate, methyl cellulose, ethyl cellulose, hydroxyethyl cellulose, ethyl hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl ethyl cellulose, microcrystalline cellulose, polyacrylamide, amino compounds of polyacrylamide, polyacrylhydrazine, acrylamide-metal acrylate copolymer, polyacrylamide-poly(acrylic acid ester) copolymer, polyvinyl alcohol, acrylic rubber, guar gum, starch, and silicone.
  • the content of the binder is preferably not more than 10 part by mass to 100 part by mass of the total of the components (A) to (C).
  • the composition of the invention may further contain an additive selected from metal oxides and metal carbonates, based on the necessity.
  • the additive may be added for the purpose to assist the function of the component (D) , that is, to decrease the combustion temperature of the composition, adjust the burning rate and suppress the production amounts of the toxic nitrogen oxide and carbon monoxide after combustion.
  • the additive may be at least one selected from metal oxides such as copper oxide, iron oxide, zinc oxide, cobalt oxide, manganese oxide, molybdenum oxide, nickel oxide, bismuth oxide, silica or alumina; metal carbonates or basic metal carbonates such as cobalt carbonate, calcium carbonate, basic zinc carbonate or basic copper carbonate; complex compounds of metal oxides or hydroxides such as Japanese acid clay, kaolin, talc, bentonite, diatomaceous earth or hydrotalcite; metal acid salts such as sodium silicate, mica molybdenic acid salt, cobalt molybdate or ammonium molybdate; molybdenum disulfide, calcium stearate, silicon nitride, and silicon carbide.
  • metal oxides such as copper oxide, iron oxide, zinc oxide, cobalt oxide, manganese oxide, molybdenum oxide, nickel oxide, bismuth oxide, silica or alumina
  • metal carbonates or basic metal carbonates such as cobalt carbonate,
  • the content of the additives is preferably not more than 10 part by mass to 100 part by mass of the total of the components (A) to (C).
  • the composition of the invention is preferable to have an oxygen balance in the range of -0.02 g/g to +0.02 g/g, more preferably -0.01 g/g to +0.01 g/g, and still more preferably -0.006 g/g to +0.006 g/g.
  • the oxygen balance is the mass (expressed as +) of oxygen produced in the case of complete combustion of 1 gram of the gas generating composition or the mass (expressed as -) of oxygen needed in the case of complete combustion and can be calculated by adding up products of the oxygen balances and the contents (% by mass) of the respective components of the gas generating composition.
  • composition of the invention can be molded into a desired shape, and it may be molded into a single-perforated cylinder, a perforated(porous) cylinder or a pellet.
  • molded articles can be produced by an extrusion-molding method (for a single-perforated cylinder and a perforated (porous) cylinder) comprising the steps of adding water or an organic solvent to the composition and extruding the mixture, or by a compression-molding method (for a pellet) comprising the steps of compressing the above mixture using a pelletizer.
  • the single-perforated cylinder and the perforated (porous) cylinder may have either of a longitudinal through-hole or a hollow without penetrating.
  • composition of the invention and molded articles obtained therefrom may be used for an inflator for a driver side, an inflator for a passenger side next to a driver seat, an inflator for a side air bag, an inflator for an inflatable curtain, an inflator for a knee bolster, an inflator for an inflatable seat belt, an inflator for a tubular system and an inflator for a pretensioner of a variety of vehicles.
  • the inflators using the composition of the invention and the molded article obtained from the composition may be a pyrotechnic type in which the gas is supplied only from gas generating agent or a hybrid type in which both of compressed gas such as argon and gas from the gas generating agent are supplied.
  • composition of the invention and the molded article obtained from the composition may be used as an igniting agent, so-called an enhancer (or a booster), for transmitting the energy of a detonator or a squib to the gas generating agent.
  • an enhancer or a booster
  • the gas generating compositions shown in Table 1 were produced. Their oxygen balances, the combustion temperatures based on the theoretical calculation, and gas outputs (the unit, mol/100 g, means the mole number of the generated gas per 100 g of each composition) were measured. The results are shown in Table 1.
  • NQ stands for nitroguanidine
  • GN stands for guanidine nitric acid
  • BCN stands for basic copper nitrate
  • CMCNa carboxymethyl cellulose sodium salt. They are similarly shown in the other tables.
  • compositions of Examples 3 and 4 were found having the friction sensitivity exceeding 353 N and the drop hammer sensitivity exceeding 60 cm, and they are insensitive in the friction sensitivity and the drop hammer sensitivity, and thus they have high handling safety.
  • 1,888.5 g of guanidine nitric acid salt, 2,269 g of basic copper nitrate, 500 g of aluminum hydroxide, 250 g of CMCNa, 100 g of sodium perchlorate, and 700 g of water were loaded to a mixer and mixed all together.
  • the mixture was extruded by an extruder, cut, and dried to obtain a single hole type gas generating composition having the outer diameter of 4.25 mm, the inner diameter of 1.10 mm, and the length of 4. 08 mm. 40.3 g of the gas generating composition was air-tightly sealed in a chamber having the inner diameter of 57 mm and the height of 32 mm to produce an inflator for a test.
  • the inflator Using the inflator, a well-known 60-liter tank test (e.g. disclosed in column 22 of JP-A No. 2001-97176) and a discharged gas test of a 2800-liter tank were carried out.
  • the 2800-liter tank test was carried out by setting the inflator in a tank made of an iron and having a capacity of 2,800 liters; igniting the inflator; measuring the concentrations of NO, NO 2 , CO and NH 3 in the tank after 3 minutes, 15 minutes, and 30 minutes from the ignition; and determining the average values of the respective moments as the respective gas concentrations.
  • the concentrations of NO, NO 2 , CO, and NH 3 shown in Table 3 were found extremely low, and thus it was confirmed that the safety to a passenger is high when the gas generating composition is burned to expand an air bag.

Abstract

To provide a gas generating composition with a good ignition property and combustibility and generating suppressed amounts of toxic gases such as NOx and ammonia at the time of combustion, the gas generating composition comprises (A) a nitrogen-containing compound as fuel, (B) a basic metal nitrate and (C) a chloric acid compound as oxidizing agents, the chloric acid compound (C) is (C-1) a perchloric acid salt and/or (C-2) a chloric acid salt and the content of the component (C) is less than 5% by mass in the total oxidizing agents.

Description

    Technical Field of the Invention
  • The invention relates to a gas generating composition to be used for a gas generator for an air bag.
  • Prior arts
  • A gas generating composition comprises fuel, an oxidizing agent and a variety of additives to be added based on the necessity, and the composition is required to satisfy that the gas generated by combustion is clean, in other words, the gas contains no nitrogen oxide (NOx), CO, or the like.
  • It has been known that basic copper nitrate (BCN) known as an oxidizing agent decreases the combustion temperature. because of low combustion heat generation and suppresses the production amount of NOx and thus has an effect to clean the discharged gas, and it also has an effect to improve the ignition and the combustion properties and therefore, it has been used widely as an oxidizing agent.
  • However, if the content of BCN as an oxidizing agent is too high, it results in a problem that the generation amounts of NOx and ammonia are adversely increased.
  • A chloric acid compound also well-known as an oxidizing agent causes NOx removal reaction and becomes a supply source of oxygen required to decompose NOx into nitrogen and water, and therefore it has been used widely.
  • However, if the content of the chloric acid compound as an oxidizing agent is too much, the supply of oxygen so exceeds as to rather increase the generation amounts of NOx and mist.
  • In EP-B No. 1, 006, 096 and US-A1 No. 2003/0145921, BCN is used as an oxidizing agent to decrease the combustion temperature and accordingly the discharged gas is cleaned and a satisfactory burning rate is obtained. However, in EP-B No. 1,006,096 and US-A1 No. 2003/0145921, the use ratio of the perchloric acid salt to BCN is high and the supply of oxygen becomes excess, so that, the generation amounts of NOx and mist are unsatisfactorily increased.
  • In US-B No. 5, 608, 183, as described in EP-B No. 1, 006, 096, neither sufficient ignition property nor burning rate can be obtained. Further, normally in this system, so much BCN is contained that the cleanness level of the discharged gas is low.
  • Summary of the Invention
  • A purpose of the invention is to provide a gas generating composition with a good ignition property and combustibility and generating suppressed amounts of toxic gases such as NOx and ammonia at the time of combustion.
  • As a means for solving the above-mentioned problems, the invention provides a gas generating composition comprising (A) a nitrogen-containing compound as fuel and (B) a basic metal nitrate and (C) a chloric acid compound as oxidizing agents, the chloric acid compound (C) being selected from (C-1) a perchloric acid salt and (C-2) a chloric acid salt, the content of the component (C) being less than 5% by mass in the total oxidizing agents.
  • Detailed explanation of the invention
  • The composition of the invention has a good ignition property and combustibility (a high burning rate) and can decrease the generation amounts of NOx and ammonia gas at the time of combustion, so that the amounts of NOx and ammonia to be contained in the combustion gas can be suppressed.
  • Therefore, if the composition of the invention is applied to a gas generator for an air bag, a necessary amount of a gas for expansion can be generated within a time to reliably protect a passenger and at the same time, the toxic gas amount can remarkably be suppressed in the gas for expanding the air bag and thus, the safety can be enhanced.
  • The fuel to be used in the invention contains a nitrogen-containing compound as the component (A), and as the nitrogen-containing compound, at least one selected from tetrazole compounds, guanidine compounds, triazine compounds and nitroamine compounds. In addition, other than the nitrogen-containing compound, known fuel may be contained and in such a case, the ratio of the nitrogen-containing compound in the fuel is preferably 20% or more by mass.
    As the tetrazoles, 5-aminotetrazole and bitetrazole ammonium are preferable. As the guanidines, guanidine nitric acid salt (nitric acid guanidine), aminoguanidine nitric acid salt, nitroguanidine, and triaminoguanidine nitric acid salt are preferable. As triazines, melamine, cyanuric acid, ammeline, ammelide, and ammeland are preferable. As nitroamines, cyclo-1,3,5-trimethine-2,4,6-trinitramine is preferable. Among them, guanidine nitric acid salt is particularly preferable.
  • The content of the component (A) is preferably 15 to 50% by mass, more preferably 20 to 55% by mass, and even more preferably 25 to 50% by mass.
  • The oxidizing agent to be used in the invention includes the basic metal nitrate (B) , the chloric acid compound (C) , and additionally other oxidizing agents to be used based on the necessity.
  • An example of the basic metal nitrate of the component (B) can be at least one of the compounds selected from basic copper nitrate, basic cobalt nitrate, basic zinc nitrate, basic manganese nitrate, basic iron nitrate, basic molybdenum nitrate, basic bismuth nitrate, and basic cerium nitrate.
  • To increase the burning rate, the basic metal nitrate is preferable to have the average particle diameter of 30 µm or smaller, more preferably 10 µm or smaller. The average particle diameter is measured according to a particle size distribution method using laser scattered beam. The measurement sample is prepared by dispersing the basic metal nitrate in water and radiating ultrasonic wave for 3 minutes, and 50% cumulative values (D50) of the particles are calculated and the average of the values measured twice is employed as the average particle diameter.
  • The chloric acid compound of the component (C) is a component having an oxidizing function and a combustion promoting function. The oxidizing function means to generate oxygen during the combustion and accordingly to efficiently promote combustion as well as to suppress the production amount of the toxic gases such as NOx, ammonia, carbon monoxide and the like. On the other hand, the combustion promoting function means to improve the ignition property of the gas generating composition or to improve the burning rate (enhancing the combustibility).
  • The chloric acid compound of the component (C) may include the perchloric acid salt (C-1) and/or the chloric acid salt (C-2).
  • The perchloric acid salt of the component (C-1) may include ammonium perchlorate, potassium perchlorate, and sodium perchlorate. The chloric acid salt of the component (C-2) may include chloric acid, potassium chlorate, and sodium chlorate, and among them, sodium perchlorate is particularly preferable.
  • The chloric acid compound of the component (C) is preferable to have the average particle diameter of 1 to 500 µm, more preferably 2 to 50 µm. The measurement method of the average particle diameter is the same as that of the average particle diameter of the component (B).
  • The total content of the oxidizing agents of the component (B) and component (C) is preferably 30 to 70% by mass, more preferably 35 to 60% by mass, and even more preferably 40 to 55% by mass in the gas generating composition.
  • The content of the component (C) in the total oxidizing agent is less than 5% by mass, preferably 1 to 5% by mass, and even more preferably 2 to 5% by mass. If the content of the component (C) is less than 5% by mass, the combustion temperature can be lowered.
  • The mass ratio (B)/(C) of the basic copper nitrate (B) and the chloric acid compound (C) in the oxidizing agents is preferably in the range of 3 to 70, more preferably 3 to 25, furthermore preferably 5 to 25, still more preferably 7 to 20, and most preferably 5 to 20.
  • If the mass ratio (B)/(C) is in the above ranges, the ignition property of the composition is improved and the combustibility (the burning rate) is also improved and at the same time, the production amounts of NOx and ammonia are suppressed at the time of the combustion and therefore, the combustion gas is clean.
  • When known oxidizing agents other than the components (B) and (C) are contained, the content of the basic copper nitrate (B) in the total oxidizing agents is 50% by mass or more, preferably 60% by mass or more, and still preferably 70% by mass or more. If the content of component (B) is in the above range, the ignition property of the composition is improved and the combustibility (the burning rate) is also improved.
  • The composition of the invention may further contain the component (D) of a metal hydroxide, a hydrated metal oxide, or a combination thereof as a coolant. The coolant has a function for lowering the combustion temperature. The component (D) greatly absorbs heat when it is thermally decomposed and produced an oxide and water. Therefore, addition of the component (D) is effective to decrease the combustion temperature of the composition and suppress the production amounts of toxic NOx and carbon monoxide.
  • An example of the metal hydroxide of the component (D) can be magnesium hydroxide, aluminum hydroxide, calcium hydroxide, zirconium hydroxide, cobalt hydroxide and copper hydroxide, and an example of the hydrated metal oxide can be hydrated aluminum oxide.
  • By adjusting an average particle diameter, the component (D) can improve the entire dispersibility when the components (A) to (C) are mixed, so that the mixing work is made easy and the ignition property of the obtained composition can be improved.
  • The average particle diameter of the component (D) is preferably 0.1 to 70 µm, more preferably 0.5 to 50 µm, and even more preferably 2 to 30 µm. The measurement method of the average particle diameter is the same measurement method of the average particle diameter of the component (B).
  • The content of the component (D) in the gas generating composition is preferably 1 to 15% by mass, more preferably 3 to 12% by mass, and even more preferably 5 to 10% by mass.
  • If necessary, the composition of the invention may contain a binder. The binder is a component to be used together with the components (A) to (C) based on the necessity and is a component to improve the formability of the composition and increase the strength of a molded article of the gas generating agent. If the strength of a molded article of the gas generating agent is insufficient, it may occur that the molded article breaks at the time of actual combustion and is burned too intensely to control the combustion.
  • The binder may be at least one compound selected from carboxymethyl cellulose, carboxymethyl cellulose sodium salt, carboxymethyl cellulose potassium salt, carboxymethyl cellulose ammonium salt, cellulose acetate, cellulose acetate butyrate, methyl cellulose, ethyl cellulose, hydroxyethyl cellulose, ethyl hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl ethyl cellulose, microcrystalline cellulose, polyacrylamide, amino compounds of polyacrylamide, polyacrylhydrazine, acrylamide-metal acrylate copolymer, polyacrylamide-poly(acrylic acid ester) copolymer, polyvinyl alcohol, acrylic rubber, guar gum, starch, and silicone.
  • The content of the binder is preferably not more than 10 part by mass to 100 part by mass of the total of the components (A) to (C).
  • The composition of the invention may further contain an additive selected from metal oxides and metal carbonates, based on the necessity. The additive may be added for the purpose to assist the function of the component (D) , that is, to decrease the combustion temperature of the composition, adjust the burning rate and suppress the production amounts of the toxic nitrogen oxide and carbon monoxide after combustion.
  • The additive may be at least one selected from metal oxides such as copper oxide, iron oxide, zinc oxide, cobalt oxide, manganese oxide, molybdenum oxide, nickel oxide, bismuth oxide, silica or alumina; metal carbonates or basic metal carbonates such as cobalt carbonate, calcium carbonate, basic zinc carbonate or basic copper carbonate; complex compounds of metal oxides or hydroxides such as Japanese acid clay, kaolin, talc, bentonite, diatomaceous earth or hydrotalcite; metal acid salts such as sodium silicate, mica molybdenic acid salt, cobalt molybdate or ammonium molybdate; molybdenum disulfide, calcium stearate, silicon nitride, and silicon carbide.
  • The content of the additives is preferably not more than 10 part by mass to 100 part by mass of the total of the components (A) to (C).
  • The composition of the invention is preferable to have an oxygen balance in the range of -0.02 g/g to +0.02 g/g, more preferably -0.01 g/g to +0.01 g/g, and still more preferably -0.006 g/g to +0.006 g/g. The oxygen balance is the mass (expressed as +) of oxygen produced in the case of complete combustion of 1 gram of the gas generating composition or the mass (expressed as -) of oxygen needed in the case of complete combustion and can be calculated by adding up products of the oxygen balances and the contents (% by mass) of the respective components of the gas generating composition.
  • If the oxygen balance is in the above range, the production amounts of NOx and ammonia can be decreased, so that the combustion gas becomes clean.
  • The composition of the invention can be molded into a desired shape, and it may be molded into a single-perforated cylinder, a perforated(porous) cylinder or a pellet.
  • These molded articles can be produced by an extrusion-molding method (for a single-perforated cylinder and a perforated (porous) cylinder) comprising the steps of adding water or an organic solvent to the composition and extruding the mixture, or by a compression-molding method (for a pellet) comprising the steps of compressing the above mixture using a pelletizer. The single-perforated cylinder and the perforated (porous) cylinder may have either of a longitudinal through-hole or a hollow without penetrating.
  • The composition of the invention and molded articles obtained therefrom may be used for an inflator for a driver side, an inflator for a passenger side next to a driver seat, an inflator for a side air bag, an inflator for an inflatable curtain, an inflator for a knee bolster, an inflator for an inflatable seat belt, an inflator for a tubular system and an inflator for a pretensioner of a variety of vehicles.
  • The inflators using the composition of the invention and the molded article obtained from the composition may be a pyrotechnic type in which the gas is supplied only from gas generating agent or a hybrid type in which both of compressed gas such as argon and gas from the gas generating agent are supplied.
  • The composition of the invention and the molded article obtained from the composition may be used as an igniting agent, so-called an enhancer (or a booster), for transmitting the energy of a detonator or a squib to the gas generating agent.
  • Examples Examples 1 and 2 and Comparative Examples 1 to 3
  • The gas generating compositions shown in Table 1 were produced. Their oxygen balances, the combustion temperatures based on the theoretical calculation, and gas outputs (the unit, mol/100 g, means the mole number of the generated gas per 100 g of each composition) were measured. The results are shown in Table 1.
    Composition (composition ratio: % by mass) Oxygen balance
    (g/g)
    Combustion temperature
    (K)
    Gas generation efficiency
    (mol/100 g)
    Comparative Example 1 NQ/Sr(NO3)2 (56.9/43.1) 0 2647 2.96
    Comparative Example 2 GN/BCN (53.4/46.6) 0 1911 3.01
    Comparative Example 3 GN/BCN/KClO4
    (56.26/33.74/10)
    0 2173 3.38
    Example 1 GN/BCN/CMCNa/KClO4
    (44.1/48.4/5/2.5)
    -0.009 1844 2.88
    Example 2 GN/BCN/CMCNa/NaClO4
    (44.37/48.13/5/2.5)
    -0.009 1856 2.89
  • In Table 1, NQ stands for nitroguanidine, GN stands for guanidine nitric acid, BCN stands for basic copper nitrate, and CMCNa stands for carboxymethyl cellulose sodium salt. They are similarly shown in the other tables.
  • The combustion temperatures of Examples 1 and 2 are lower than those of corresponding Comparative Examples 1 to 3.
  • Examples 3 and 4
  • The gas generating compositions shown in Table 2 were produced. The friction sensitivity test and drop hammer sensitivity test with respect to the compositions were conducted according to the explosive performance test method of JIS K4810-1979. The results are shown in Table 2.
    Composition
    (composition ratio: % by mass)
    Friction sensitivity
    (N)
    Drop hammer sensitivity
    (cm)
    Example 3 GN/BCN/CMCNa/KClO4 (44.1/48.4/5/2.5) >353 >600
    Example 4 GN/BCN/CMCNa/NaClO4 (44.37/48.13/5/2.5) >353 >60
  • The compositions of Examples 3 and 4 were found having the friction sensitivity exceeding 353 N and the drop hammer sensitivity exceeding 60 cm, and they are insensitive in the friction sensitivity and the drop hammer sensitivity, and thus they have high handling safety.
  • Example 5
  • 1,888.5 g of guanidine nitric acid salt, 2,269 g of basic copper nitrate, 500 g of aluminum hydroxide, 250 g of CMCNa, 100 g of sodium perchlorate, and 700 g of water were loaded to a mixer and mixed all together. The mixture was extruded by an extruder, cut, and dried to obtain a single hole type gas generating composition having the outer diameter of 4.25 mm, the inner diameter of 1.10 mm, and the length of 4. 08 mm. 40.3 g of the gas generating composition was air-tightly sealed in a chamber having the inner diameter of 57 mm and the height of 32 mm to produce an inflator for a test.
  • Using the inflator, a well-known 60-liter tank test (e.g. disclosed in column 22 of JP-A No. 2001-97176) and a discharged gas test of a 2800-liter tank were carried out. The 2800-liter tank test was carried out by setting the inflator in a tank made of an iron and having a capacity of 2,800 liters; igniting the inflator; measuring the concentrations of NO, NO2, CO and NH3 in the tank after 3 minutes, 15 minutes, and 30 minutes from the ignition; and determining the average values of the respective moments as the respective gas concentrations.
  • As a result, in the 60-liter tank test, the inner pressure of the inflator was 16.8 MPa and the tank pressure was 185.2 KPa and these values were satisfying the conditions for practical use. The result of the 2800-liter tank test is shown in Table 3.
    NO2 NO CO NH3
    Discharged gas concentration
    (ppm: on the basis of mole number)
    0 7 70 8.5
  • The concentrations of NO, NO2, CO, and NH3 shown in Table 3 were found extremely low, and thus it was confirmed that the safety to a passenger is high when the gas generating composition is burned to expand an air bag.

Claims (6)

  1. A gas generating composition comprising (A) a nitrogen-containing compound as fuel and (B) a basic metal nitrate and (C) a chloric acid compound as oxidizing agents, the chloric acid compound (C) being at least one selected from group consisting of (C-1) a perchloric acid salt and (C-2) a chloric acid salt, the content of the component (C) being less than 5% by mass in the total oxidizing agents.
  2. The gas generating composition as claimed in claim 1, wherein the component (B) is a basic copper nitrate and the perchloric acid salt (C-1) is sodium perchlorate or potassium perchlorate and the chloric acid salt (C-2) is sodium chlorate or potassium chlorate.
  3. The gas generating composition as claimed in claim 1 or 2, wherein the average particle diameter of the chloric acid compound (C) is 1 to 500 µm.
  4. The gas generating composition as claimed in any one of claims 1 to 3, further comprising (D) a metal hydroxide, a hydrate of a metal oxide or a combination thereof.
  5. The gas generating composition as claimed in claim 4, wherein the metal hydroxide (D) is magnesium hydroxide.
  6. The gas generating composition as claimed in any one of claims 1 to 5, having an oxygen balance in the range of -0.02 g/g to +0.02 g/g.
EP04024216.6A 2003-10-20 2004-10-11 Gas generating composition Active EP1526121B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2003358774A JP4767487B2 (en) 2003-10-20 2003-10-20 Gas generant composition
JP2003358774 2003-10-20

Publications (2)

Publication Number Publication Date
EP1526121A1 true EP1526121A1 (en) 2005-04-27
EP1526121B1 EP1526121B1 (en) 2019-05-08

Family

ID=34386451

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04024216.6A Active EP1526121B1 (en) 2003-10-20 2004-10-11 Gas generating composition

Country Status (4)

Country Link
EP (1) EP1526121B1 (en)
JP (1) JP4767487B2 (en)
CN (1) CN100391911C (en)
CA (1) CA2485370A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2892117A1 (en) * 2005-10-13 2007-04-20 Snpe Materiaux Energetiques Sa FAST GAS GENERATING PYROTECHNIC COMPOSITION AND PROCESS FOR OBTAINING THE SAME
EP2061736A1 (en) * 2006-08-28 2009-05-27 Autoliv Asp, Inc. Extrudable gas generant
WO2011030071A2 (en) 2009-09-10 2011-03-17 Snpe Materiaux Energetiques Gas-generating pyrotechnic compounds
EP2407443A1 (en) * 2009-03-13 2012-01-18 Nipponkayaku Kabushikikaisha Gas generant composition, molded object thereof, and gas generator using same
WO2012035271A2 (en) 2010-09-15 2012-03-22 Sme Pyrotechnic gas generator compounds

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5274078B2 (en) * 2008-04-02 2013-08-28 株式会社ダイセル Gas generant composition
JP5663369B2 (en) 2011-03-31 2015-02-04 株式会社ダイセル Gas generant composition
JP6352134B2 (en) * 2014-09-29 2018-07-04 株式会社ダイセル Ignition composition
DE102016203058B3 (en) * 2016-02-26 2017-05-18 Heraeus Deutschland GmbH & Co. KG Copper-ceramic composite and module
WO2022071462A1 (en) * 2020-10-01 2022-04-07 株式会社ダイセル Gas-generating agent composition
CN114044729A (en) * 2021-11-16 2022-02-15 湖北航鹏化学动力科技有限责任公司 Gas generating agent composition, gas generating agent, preparation method and application
CN115959957A (en) * 2022-08-25 2023-04-14 南京理工大学 Method for preparing gas generating agent composition by using waste basic copper nitrate and application
CN115894138A (en) * 2022-08-25 2023-04-04 南京理工大学 Method for recycling waste copper nitrate containing guanidine alkali and application

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4386979A (en) * 1979-07-19 1983-06-07 Jackson Jr Charles H Gas generating compositions
EP0509763A1 (en) * 1991-04-15 1992-10-21 Automotive Systems Laboratory Inc. Method of controlling the amount of oxides of nitrogen in generated gas for airbags
DE19643468A1 (en) * 1996-10-22 1998-04-23 Temic Bayern Chem Airbag Gmbh Gas-generating, azide-free solid mixture
DE29806504U1 (en) * 1998-04-08 1998-08-06 Trw Airbag Sys Gmbh & Co Kg Azide-free, gas generating composition
DE29821541U1 (en) * 1998-12-02 1999-02-18 Trw Airbag Sys Gmbh & Co Kg Azide-free, gas generating composition
EP1241138A1 (en) * 1999-09-27 2002-09-18 Daicel Chemical Industries, Ltd. Basic metal nitrate, method for producing the same and gas-generating agent composition
DE10225660A1 (en) * 2001-06-20 2003-02-13 Trw Inc Gas producing material, useful for automobile passenger protection during collision, includes hydroxy-terminated polybutadiene, particulate oxidizing agent, diisocyanate crosslinker, an elastomer binder and catalysts
US20030145921A1 (en) * 2001-12-27 2003-08-07 Trw Inc. Cool burning gas generating material for a vehicle occupant protection apparatus

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5439537A (en) * 1993-08-10 1995-08-08 Thiokol Corporation Thermite compositions for use as gas generants
JP4332936B2 (en) * 1998-07-13 2009-09-16 日油株式会社 Gas generating composition and molded product thereof
JP2000226291A (en) * 1999-02-03 2000-08-15 Daicel Chem Ind Ltd Airbag gas-generating agent composition and formed body both for reducing injuriousness to crew and passenger
DE19932466A1 (en) * 1999-07-12 2001-01-18 Trw Airbag Sys Gmbh & Co Kg Azide free gas generating composition
JP4800469B2 (en) * 1999-10-08 2011-10-26 ダイセル化学工業株式会社 Gas generant composition
JP4013540B2 (en) * 2000-12-27 2007-11-28 日本油脂株式会社 Gas generant composition
US6599379B2 (en) * 2001-04-12 2003-07-29 Dmd Systems, Llc Low-smoke nitroguanidine and nitrocellulose based pyrotechnic compositions
JP4244596B2 (en) * 2002-08-23 2009-03-25 日油株式会社 Gas generator
US20050016646A1 (en) * 2003-07-25 2005-01-27 Barnes Michael W. Chlorine-containing gas generant compositions including a copper-containing chlorine scavenger

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4386979A (en) * 1979-07-19 1983-06-07 Jackson Jr Charles H Gas generating compositions
EP0509763A1 (en) * 1991-04-15 1992-10-21 Automotive Systems Laboratory Inc. Method of controlling the amount of oxides of nitrogen in generated gas for airbags
DE19643468A1 (en) * 1996-10-22 1998-04-23 Temic Bayern Chem Airbag Gmbh Gas-generating, azide-free solid mixture
DE29806504U1 (en) * 1998-04-08 1998-08-06 Trw Airbag Sys Gmbh & Co Kg Azide-free, gas generating composition
DE29821541U1 (en) * 1998-12-02 1999-02-18 Trw Airbag Sys Gmbh & Co Kg Azide-free, gas generating composition
EP1241138A1 (en) * 1999-09-27 2002-09-18 Daicel Chemical Industries, Ltd. Basic metal nitrate, method for producing the same and gas-generating agent composition
DE10225660A1 (en) * 2001-06-20 2003-02-13 Trw Inc Gas producing material, useful for automobile passenger protection during collision, includes hydroxy-terminated polybutadiene, particulate oxidizing agent, diisocyanate crosslinker, an elastomer binder and catalysts
US20030145921A1 (en) * 2001-12-27 2003-08-07 Trw Inc. Cool burning gas generating material for a vehicle occupant protection apparatus

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2892117A1 (en) * 2005-10-13 2007-04-20 Snpe Materiaux Energetiques Sa FAST GAS GENERATING PYROTECHNIC COMPOSITION AND PROCESS FOR OBTAINING THE SAME
WO2007042735A3 (en) * 2005-10-13 2007-06-21 Snpe Materiaux Energetiques Rapid gas generating pyrotechnical composition and method for obtaining same
CN101312930B (en) * 2005-10-13 2013-01-16 Snpe巨能材料公司 Rapid gas generating pyrotechnical composition and method for obtaining same
EP2061736A1 (en) * 2006-08-28 2009-05-27 Autoliv Asp, Inc. Extrudable gas generant
EP2061736A4 (en) * 2006-08-28 2013-11-27 Autoliv Asp Inc Extrudable gas generant
EP2407443A1 (en) * 2009-03-13 2012-01-18 Nipponkayaku Kabushikikaisha Gas generant composition, molded object thereof, and gas generator using same
EP2407443A4 (en) * 2009-03-13 2013-11-27 Nippon Kayaku Kk Gas generant composition, molded object thereof, and gas generator using same
WO2011030071A2 (en) 2009-09-10 2011-03-17 Snpe Materiaux Energetiques Gas-generating pyrotechnic compounds
WO2012035271A2 (en) 2010-09-15 2012-03-22 Sme Pyrotechnic gas generator compounds

Also Published As

Publication number Publication date
CA2485370A1 (en) 2005-04-20
CN100391911C (en) 2008-06-04
JP4767487B2 (en) 2011-09-07
EP1526121B1 (en) 2019-05-08
JP2005119926A (en) 2005-05-12
CN1609080A (en) 2005-04-27

Similar Documents

Publication Publication Date Title
EP0880485B1 (en) Nonazide gas generating compositions
US6210505B1 (en) High gas yield non-azide gas generants
JP4302442B2 (en) Gas generant composition
KR100838192B1 (en) Gas-generating agent composition comprising triazine derivative
US6964716B2 (en) Gas generating composition
EP2444383B1 (en) Gas generant composition
US9487454B2 (en) Gas generating composition
US20100078098A1 (en) Gas generating composition for inflator containing melamine cyanurate
EP1526121B1 (en) Gas generating composition
US20050127324A1 (en) Gas generating composition
US20040016480A1 (en) Nonazide gas generant compositions
JP4672974B2 (en) Gas generant composition
US8137771B2 (en) Gas generating composition
US20060191614A1 (en) Gas generating composition
US20050098247A1 (en) Gas generating composition
US7887650B2 (en) Gas generating composition
US20050155681A1 (en) Gas generating composition
EP1816113B1 (en) Gas generating composition
JP4794813B2 (en) Gas generant composition
US20040154710A1 (en) Gas generating composition
KR100456410B1 (en) Gas generant for air bag
CA2318766A1 (en) High gas yield non-azide gas generants

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL HR LT LV MK

17P Request for examination filed

Effective date: 20050707

AKX Designation fees paid

Designated state(s): DE FR SE

17Q First examination report despatched

Effective date: 20071121

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: DAICEL CHEMICAL INDUSTRIES, LTD.

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20190108

RIC1 Information provided on ipc code assigned before grant

Ipc: C06D 5/06 20060101AFI20041207BHEP

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR SE

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602004053945

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190508

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602004053945

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed

Effective date: 20200211

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20191031

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20231020

Year of fee payment: 20