US3719604A - Pressurizing-gas-producing charges containing an aminoguanidine tetrazole and an oxygen-liberating or gas-evolving additive - Google Patents

Pressurizing-gas-producing charges containing an aminoguanidine tetrazole and an oxygen-liberating or gas-evolving additive Download PDF

Info

Publication number
US3719604A
US3719604A US00110601A US3719604DA US3719604A US 3719604 A US3719604 A US 3719604A US 00110601 A US00110601 A US 00110601A US 3719604D A US3719604D A US 3719604DA US 3719604 A US3719604 A US 3719604A
Authority
US
United States
Prior art keywords
gas
liberating
composition
oxygen
group
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.)
Expired - Lifetime
Application number
US00110601A
Inventor
J Prior
W Siegelin
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.)
Dynamit Nobel AG
Original Assignee
Dynamit Nobel AG
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 Dynamit Nobel AG filed Critical Dynamit Nobel AG
Application granted granted Critical
Publication of US3719604A publication Critical patent/US3719604A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B43/00Compositions characterised by explosive or thermic constituents not provided for in groups C06B25/00 - C06B41/00

Definitions

  • These materials may also consist of mixtures of oxygenliberating substances, such as potassium chlorate, and gas-evolving substances such as ammonium nitrate or guanidine nitrate. (See, for example, German patents 854,770, 851,919, and 909,424.)
  • one aspect of this invention resides in novel pressurizinggas-producing charges, particularly for use in pressurizing-gas-actuated devices, which are characterized by the fact that they comprise from 40 to 100 weight percent aminoguanidine salts of azotetrazole and/or ditetrazole.
  • Other components of the composition may include oxygen-liberating and/or other gas-evolving substances which do not cause detonation. These may be used singly or in combination in proportion of 0 to 60 weight percent.
  • Azotetrazole has the formula and ditetrazole has the formula N N 111 1 I l
  • the hydrogen atoms of these compounds have an acid reaction and consequently form, with aminoguanidine, the corresponding salts.
  • These salts are prepared, for example, by mixing aqueous solutions of salts of aminoguanidine, such as aminoguanidine sulfate, with aqueous solutions of alkali salts of said tetrazoles.
  • the insoluble salt compounds suitable for use in accordance with the present invention precipitate from this reaction mixture and can be recovered by conventional chemical engineering techniques.
  • Suitable oxygen-liberating optional additives are chlorates, perchlorates and nitrates of inorganic bases which are all preferred. Nitroguanidine, guanidine nitrate, nitrocellulose, nitropolystyrene, polynitrophenols, polynitrocresols or the like can also be incorporated as oxygen liberators.
  • Soleiy gas-evolving optional additives which are suitable are, for example, ammonium oxalate, urea, aminoguanidine, sugar, tartaric acid or the like.
  • Catalysts promoting decomposition such as compounds of vanadium, tungsten, molybdenum, chromium, cobalt or the like, particularly in the highest degree of oxidation of the metal, may advantageously be added to the compositions of this invention in a proportion of from 0.5 to 5 weight percent, referred to the total mixture.
  • compositions of this invention are prepared by simple mixing of the ingredients.
  • the resultant solid composition may be pressed, but this is not absolutely necessary.
  • EXAMPLE 1 A mixture of 500 g of azotetrazole-aminoguanidine salt and 500 g of barium nitrate was pressed into bodies which were then ignited in a pressure pipe with nozzle. A strong gas jet was thus produced. The mixture furnished 350 cc gas/g of mixture. It was not ignited by the shock of a falling weight of 2 kg dropped from a height of 2 meters.
  • EXAMPLE 2 An intimate mixture of 700 g of ditetrazoleaminoguanidine salt and 300 g of potassium nitrate was pressed into bodies which were ignited in a pressure pipe with nozzle by the use of an electric primer pellet. The quantity of gas evolved was 400 cc/g. The mixture was not ignited by the shock of a falling weight of 2 kg dropped from a height of 2 meters.
  • a pressure composition was prepared from 50 g of barium nitrate (Ba(NO 50 g of azotetrazoleaminoguanidine salt, 4 g of vanadium pentoxide V 0 and 15 g of an aluminum-titanium alloy. After ignition of the composition by means of an ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 768 cal/g.
  • barium nitrate Ba(NO 50 g of azotetrazoleaminoguanidine salt, 4 g of vanadium pentoxide V 0 and 15 g of an aluminum-titanium alloy.
  • EXAMPLE 4 A pressure composition was prepared from 40 g of barium nitrate (Ba(NO and 60 g of azotetrazoleaminoguanidine salt. After ignition of the composition by means of the ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 613 cal/g, Volumer, of evolved gas: 440 em /g.
  • EXAMPLE 5 A pressure composition was prepared from 45 g of barium nitrate (Ba(NO 45 g of azotetrazoleaminoguanidine salt and g of amorphous boron. After ignition of the composition by means of the ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 826 cal/g, amount of evolved gas: 520 em /g.
  • EXAMPLE 6 A pressure composition was prepared from 30 g of barium nitrate (Ba(NO 50 g of azotetrazoleaminoguanidine salt and g of potassium nitrate (K- NO After ignition of the composition by means of the ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 687 cal/g.
  • a gas-producing composition comprising an aminoguanidine salt of at least one member selected from the group consisting of azotetrazole of the formula:
  • II-N N and an oxygen-liberating additive or a gas-evolving additive selected from the group consisting of ammonium oxalate, urea, aminoguanidine, sugar and tartaric acid present in an amount up to 60 weight percent of the composition.
  • an oxygen-liberating additive or a gas-evolving additive selected from the group consisting of ammonium oxalate, urea, aminoguanidine, sugar and tartaric acid present in an amount up to 60 weight percent of the composition.
  • oxygen-liberating additive is a member selected from 5 the group consisting of inorganic chlorates, perchlorates and nitrates; nitroguanidine; guanidine nitrate; nitrocellulose; nitropolystyrene;
  • an oxygen-liberating additive or a gas-evolving additive selected from the group consisting of ammonium oxalate, urea, aminoguanidine, sugar, and tartaric acid present in an amount up to 60 weight percent of the composition.
  • oxygen-liberating additive is a member selected from the group consisting of inorganic chlorates, perchlorates and nitrates nitroguanidine; guanidine nitrate; nitropolystyrene; nitrocellulose; polynitrophenols; and polynitrocresols.
  • oxygen-liberating or gas-evolving substance additionally contains about 0.5 to 5 weight percent, referred to the entire composition, of a metal compound catalyst wherein said metal is a member selected from the group consisting of vanadium, tungsten, molybdenum, chromium and cobalt.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Air Bags (AREA)
  • Feeding, Discharge, Calcimining, Fusing, And Gas-Generation Devices (AREA)
  • Catalysts (AREA)
  • Treating Waste Gases (AREA)

Abstract

Novel gas-generating compositions comprising 40 to 100 weight percent aminoguanidine salts of azotetrazole of the formula:

OR OF DITETRAZOLE OF THE FORMULA:

Optional other components of such compositions include oxygenliberating or other gas-evolving substances which may be present in 0 to 60 weight percent of the composition. There are also disclosed pressurizing gas-actuated devices utilizing these compositions.

Description

United States Patent 11 1 1111 3,719,604 Prior et al. 1 March 6, 1973 PRESSURIZlNG-GAS-PRODUCING [57] ABSTRACT CHARGES CONTAINING AN Novel gas-generating compositions comprising 40 to AMINOGUANIDINE TETRAZOLE AND 100 weight percent aminoguanidine salts of AN OXYGEN-LIBERATING OR GAS- azotetrazole of the formula:
EVOLVING ADDITIVE 1 Inventors 2921121 95521, reiiqqr allls q ml Siegelin, Nuremberg, both of o Germany 'll, [73] Assignee: Dynamit Nobel AG, Troisdorf, Ger- N many [22] Filed: Jan. 28, 1971 f f 21 Appl. No.: 110,601
or of ditetrazole of the formula:
[30] Foreign Application Priority Data qw;
| Feb. 3, 1970 Germany ..P 20 04 620.2
c [52] U.S. Cl. ..252/186, 23/281, 252/187, (1
252/4, 252/350, 252/372, 260/157, 260/308, 423/235, 423/240 [51] Int. Cl. ..C06 d 5/00 [58] Field of Search ..252/l86, 187,372, 350, 4; o I h f h 23/28l2; 260/57 308;,23/235 240 ptiona 0t er components 0 sue compos tions mclude oxygen-liberating or other gas-evolving substances which may be present in 0 to 60 weight per- [56] References Cited cent of the composition. There are also disclosed pres- FOREIGN PATENTS OR APPLICATIONS surizing gas-actuated devices utilizing these compositions. 854,770 11/1952 Germany 909,424 4/1954 Germany Primary Examiner- Herbefi i 3 Gig/5f Assistant Examiner-Irwin Gluck AttorneyBurgess, Dinklage & Sprung S Claims, No Drawings PRESSURlZlNG-GAS-PRODUCING CHARGES CONTAINING AN AMINOGUANIDINE TETRAZOLE AND AN OXYGEN-LIBERATING R GAS-EVOLVING ADDITIVE This invention relates to gas-evolving systems. lt more particularly refers to novel gas-evolving systems which are relatively safe from detonation and explosion.
The energy of gases liberated in a chemical reaction is utilized in industry to force liquids or solids out of a container, for example, in fire extinguishes. Other devices make use of this force to actuate slide bars or bolts or to do other work. (See, for example, German patent 854,770, introduction.) 7 7 7 As gas-generating charges, substances or mixtures are known for this purpose which are formulated entirely or largely from combustible, gasand heat-evolving 1 substances. Such substances, for example, as nitrocellulose powder or nitropolystyrene, are capable of burning without any independent feed of oxygen. These materials may also consist of mixtures of oxygenliberating substances, such as potassium chlorate, and gas-evolving substances such as ammonium nitrate or guanidine nitrate. (See, for example, German patents 854,770, 851,919, and 909,424.)
Often the heat generated in these gas-evolving reactions is undesirable, and mixtures have therefore come into use which absorb the heat evolved on oxidation by a concurrent endothermal process. Such mixtures conrain, for example, ammonium oxalate, or hydrocarbons which decompose in an endothermal reaction, such as cyclopentadiene. (German patents 882,825, and 1,150,914), respectively.)
What is desired in all cases is the evolution of as large a quantity of gas as possible, without the explosive spontaneous decomposition of the charge during such gas evolution, and maximum safety in handling, that is to say, a high degree of insensitivity to ignition by friction and shock. In contrast to this desideratum, mixture containing fairly high proportions of guanidine nitrate, for example, have a tendency to explosively decompose, which may result in destruction of the container.
It is therefore an object of this invention to provide a novel gas-generating composition.
Other and additional objects of this invention will become apparent from a consideration of this entire specification, including the claims hereof.
In accord with, and fulfilling these objects, one aspect of this invention resides in novel pressurizinggas-producing charges, particularly for use in pressurizing-gas-actuated devices, which are characterized by the fact that they comprise from 40 to 100 weight percent aminoguanidine salts of azotetrazole and/or ditetrazole. Other components of the composition may include oxygen-liberating and/or other gas-evolving substances which do not cause detonation. These may be used singly or in combination in proportion of 0 to 60 weight percent.
Azotetrazole has the formula and ditetrazole has the formula N N 111 1 I l The hydrogen atoms of these compounds have an acid reaction and consequently form, with aminoguanidine, the corresponding salts. These salts are prepared, for example, by mixing aqueous solutions of salts of aminoguanidine, such as aminoguanidine sulfate, with aqueous solutions of alkali salts of said tetrazoles. The insoluble salt compounds suitable for use in accordance with the present invention precipitate from this reaction mixture and can be recovered by conventional chemical engineering techniques.
Suitable oxygen-liberating optional additives are chlorates, perchlorates and nitrates of inorganic bases which are all preferred. Nitroguanidine, guanidine nitrate, nitrocellulose, nitropolystyrene, polynitrophenols, polynitrocresols or the like can also be incorporated as oxygen liberators.
Soleiy gas-evolving optional additives which are suitable are, for example, ammonium oxalate, urea, aminoguanidine, sugar, tartaric acid or the like.
Catalysts promoting decomposition, such as compounds of vanadium, tungsten, molybdenum, chromium, cobalt or the like, particularly in the highest degree of oxidation of the metal, may advantageously be added to the compositions of this invention in a proportion of from 0.5 to 5 weight percent, referred to the total mixture.
The compositions of this invention are prepared by simple mixing of the ingredients. The resultant solid composition may be pressed, but this is not absolutely necessary.
The following examples serve to illustrate this invention without being in any way limiting thereon.
EXAMPLE 1 A mixture of 500 g of azotetrazole-aminoguanidine salt and 500 g of barium nitrate was pressed into bodies which were then ignited in a pressure pipe with nozzle. A strong gas jet was thus produced. The mixture furnished 350 cc gas/g of mixture. It was not ignited by the shock of a falling weight of 2 kg dropped from a height of 2 meters.
EXAMPLE 2 An intimate mixture of 700 g of ditetrazoleaminoguanidine salt and 300 g of potassium nitrate was pressed into bodies which were ignited in a pressure pipe with nozzle by the use of an electric primer pellet. The quantity of gas evolved was 400 cc/g. The mixture was not ignited by the shock of a falling weight of 2 kg dropped from a height of 2 meters.
EXAMPLE 3 A pressure composition was prepared from 50 g of barium nitrate (Ba(NO 50 g of azotetrazoleaminoguanidine salt, 4 g of vanadium pentoxide V 0 and 15 g of an aluminum-titanium alloy. After ignition of the composition by means of an ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 768 cal/g.
EXAMPLE 4 A pressure composition was prepared from 40 g of barium nitrate (Ba(NO and 60 g of azotetrazoleaminoguanidine salt. After ignition of the composition by means of the ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 613 cal/g, Volumer, of evolved gas: 440 em /g.
EXAMPLE 5 A pressure composition was prepared from 45 g of barium nitrate (Ba(NO 45 g of azotetrazoleaminoguanidine salt and g of amorphous boron. After ignition of the composition by means of the ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 826 cal/g, amount of evolved gas: 520 em /g.
EXAMPLE 6 A pressure composition was prepared from 30 g of barium nitrate (Ba(NO 50 g of azotetrazoleaminoguanidine salt and g of potassium nitrate (K- NO After ignition of the composition by means of the ignition mixture disposed in a central ignition tube, a reaction of the composition set in with evolution of heat. The heat generated was 687 cal/g.
What is claimed is:
1. A gas-producing composition comprising an aminoguanidine salt of at least one member selected from the group consisting of azotetrazole of the formula:
V; HN\ //N f N II o N=N and ditetrazole of the formula:
T| II-N N and an oxygen-liberating additive or a gas-evolving additive selected from the group consisting of ammonium oxalate, urea, aminoguanidine, sugar and tartaric acid present in an amount up to 60 weight percent of the composition.
2. A composition as claimed in claim 1, wherein said oxygen-liberating additive is a member selected from 5 the group consisting of inorganic chlorates, perchlorates and nitrates; nitroguanidine; guanidine nitrate; nitrocellulose; nitropolystyrene;
polynitrophenols; and polynitrocresols.
3. A composition as claimed in claim 1, additionally containing about 0.5 to 5 weight percent, referred to the entire composition, of a metal compound catalyst wherein said metal is a member selected from the group consisting of vanadium, tungsten, molybdenum,
4. A composition as claimed in claim 3, wherein said metal is in its highest valence state. 7
5. In a process for liberating gas under pressure in which a charge comprising an oxygen-liberating or gasevolving mixture is ignited, the improvement to reduce explosive spontaneous decomposition of the charge and improve safety in handling which comprises adding to said charge an aminoguanidine salt of at leastone member selected from the group consisting of azotetrazole of the formula:
1 N=N Ha: 1i
C it C' H-N N 1:1
and ditetrazole of the formula:
and an oxygen-liberating additive or a gas-evolving additive selected from the group consisting of ammonium oxalate, urea, aminoguanidine, sugar, and tartaric acid present in an amount up to 60 weight percent of the composition.
6. An improvement according to claim 5 wherein the oxygen-liberating additive is a member selected from the group consisting of inorganic chlorates, perchlorates and nitrates nitroguanidine; guanidine nitrate; nitropolystyrene; nitrocellulose; polynitrophenols; and polynitrocresols.
7. An improvement according to claim 5 wherein the oxygen-liberating or gas-evolving substance additionally contains about 0.5 to 5 weight percent, referred to the entire composition, of a metal compound catalyst wherein said metal is a member selected from the group consisting of vanadium, tungsten, molybdenum, chromium and cobalt.
8. An improvement according to claim 7 wherein said metal is in its highest valence state.

Claims (7)

1. A gas-producing composition comprising an aminoguanidine salt of at least one member selected from the group consisting of azotetrazole of the formula:
2. A composition as claimed in claim 1, wherein said oxygen-liberating additive is a member selected from the group consisting of inorganic chlorates, perchlorates and nitrates; nitroguanidine; guanidine nitrate; nitrocellulose; nitropolystyrene; polynitrophenols; and polynitrocresols.
3. A composition as claimed in claim 1, additionally containing about 0.5 to 5 weight percent, referred to the entire composition, of a metal compound catalyst wherein said metal is a member selected from the group consisting of vanadium, tungsten, molybdenum, chromium and cobalt.
4. A composition as claimed in claim 3, wherein said metal is in its highest valence state.
5. In a process for liberating gas under pressure in which a charge comprising an oxygen-liberating or gas-evolving mixture is ignited, the improvement to reduce explosive spontaneous decomposition of the charge and improve safety in handling which comprises adding to said charge an aminoguanidine salt of at least one member selected from the group consisting of azotetrazole of the formula:
6. An improvement according to claim 5 wherein the oxygen-liberating additive is a member selected from the group consisting of inorganic chlorates, perchlorates and nitrates nitroguanidine; guanidine nitrate; nitropolystyrene; nitrocellulose; polynitrophenols; and polynitrocresols.
7. An improvement according to claim 5 wherein the oxygen-liberating or gas-evolving substance additionally contains about 0.5 to 5 weight percent, referred to the entire composition, of a metal compound catalyst wherein said metal is a member selected from the group consisting of vanadium, tungsten, molybdenum, chromium and cobalt.
US00110601A 1970-02-03 1971-01-28 Pressurizing-gas-producing charges containing an aminoguanidine tetrazole and an oxygen-liberating or gas-evolving additive Expired - Lifetime US3719604A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2004620A DE2004620C3 (en) 1970-02-03 1970-02-03 Compressed gas generating charges

Publications (1)

Publication Number Publication Date
US3719604A true US3719604A (en) 1973-03-06

Family

ID=5761179

Family Applications (1)

Application Number Title Priority Date Filing Date
US00110601A Expired - Lifetime US3719604A (en) 1970-02-03 1971-01-28 Pressurizing-gas-producing charges containing an aminoguanidine tetrazole and an oxygen-liberating or gas-evolving additive

Country Status (5)

Country Link
US (1) US3719604A (en)
CA (1) CA981024A (en)
DE (1) DE2004620C3 (en)
FR (1) FR2078084A5 (en)
GB (1) GB1313619A (en)

Cited By (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USB235011I5 (en) * 1971-03-16 1975-01-28
EP0055547A1 (en) * 1980-12-31 1982-07-07 Morton Thiokol, Inc. Solid compositions for generating nitrogen, the generation of nitrogen therefrom and inflation of gas bags therewith
US4601344A (en) * 1983-09-29 1986-07-22 The United States Of America As Represented By The Secretary Of The Navy Pyrotechnic fire extinguishing method
US5015309A (en) * 1989-05-04 1991-05-14 Morton International, Inc. Gas generant compositions containing salts of 5-nitrobarbituric acid, salts of nitroorotic acid, or 5-nitrouracil
US5053086A (en) * 1985-03-15 1991-10-01 The United States Of America As Represented By The Secretary Of The Navy Gas generant compositions containing energetic high nitrogen binders
US5160386A (en) * 1991-11-04 1992-11-03 Morton International, Inc. Gas generant formulations containing poly(nitrito) metal complexes as oxidants and method
US5198046A (en) * 1991-03-14 1993-03-30 Fraunhofer-Gesellschaft Zur Forderung Der Angewandten Forschund E.V. Stable, nitrogen-rich composition
US5197758A (en) * 1991-10-09 1993-03-30 Morton International, Inc. Non-azide gas generant formulation, method, and apparatus
WO1995004015A1 (en) * 1993-08-02 1995-02-09 Thiokol Corporation Bitetrazoleamine gas generant compositions and methods of use
WO1995004016A1 (en) * 1993-08-02 1995-02-09 Thiokol Corporation Anhydrous tetrazole gas generant compositions and methods of preparation
WO1995004014A1 (en) * 1993-08-02 1995-02-09 Thiokol Corporation Method for preparing anhydrous tetrazole gas generant compositions
WO1995004710A1 (en) * 1993-08-04 1995-02-16 Automotive Systems Laboratory, Inc. Law residue azide-free gas generant composition
US5425886A (en) * 1993-06-23 1995-06-20 The United States Of America As Represented By The Secretary Of The Navy On demand, non-halon, fire extinguishing systems
US5428165A (en) * 1994-01-06 1995-06-27 Thiokol Corporation Process for making 5-introbarbituric acid and salts thereof
WO1995019341A2 (en) * 1994-01-06 1995-07-20 Thiokol Corporation Process for making 5-nitrobarbituric acid and salts thereof
US5439251A (en) * 1992-11-30 1995-08-08 Toyo Kasei Kogyo Company Limited Method of tetrazole amine salts having improved physical properties for generating gas in airbags
US5451682A (en) * 1994-01-10 1995-09-19 Thiokol Corporation Method for synthesizing 5-aminotetrazole
US5468866A (en) * 1994-01-04 1995-11-21 Thiokol Corporation Methods for synthesizing and processing bis-(1(2)H-tetrazol-5-yl)-amine
US5514230A (en) * 1995-04-14 1996-05-07 Automotive Systems Laboratory, Inc. Nonazide gas generating compositions with a built-in catalyst
US5516377A (en) * 1994-01-10 1996-05-14 Thiokol Corporation Gas generating compositions based on salts of 5-nitraminotetrazole
US5538567A (en) * 1994-03-18 1996-07-23 Olin Corporation Gas generating propellant
US5641938A (en) * 1995-03-03 1997-06-24 Primex Technologies, Inc. Thermally stable gas generating composition
US5661261A (en) * 1996-02-23 1997-08-26 Breed Automotive Technology, Inc. Gas generating composition
US5783773A (en) * 1992-04-13 1998-07-21 Automotive Systems Laboratory Inc. Low-residue azide-free gas generant composition
US5844164A (en) * 1996-02-23 1998-12-01 Breed Automotive Technologies, Inc. Gas generating device with specific composition
US5866842A (en) * 1996-07-18 1999-02-02 Primex Technologies, Inc. Low temperature autoigniting propellant composition
US5872329A (en) * 1996-11-08 1999-02-16 Automotive Systems Laboratory, Inc. Nonazide gas generant compositions
WO1999046222A2 (en) * 1998-03-12 1999-09-16 Automotive Systems Laboratory, Inc. High gas yield non-azide gas generants
US6306232B1 (en) 1996-07-29 2001-10-23 Automotive Systems Laboratory, Inc. Thermally stable nonazide automotive airbag propellants
US6645325B1 (en) * 1998-06-01 2003-11-11 Russell R. Nickel Fast-burning nitrocellulose compositions
US6764562B1 (en) 1999-05-12 2004-07-20 Bofors Bepab Ab Composite gas-generating material for gas-actuated car safety devices
US20040154711A1 (en) * 1998-12-30 2004-08-12 Per Sjoberg Gas-generating material for gas-actuated car safety devices
US20050257866A1 (en) * 2004-03-29 2005-11-24 Williams Graylon K Gas generant and manufacturing method thereof
WO2006128910A1 (en) * 2005-06-02 2006-12-07 Ruag Ammotec Gmbh Pyrotechnic agent
US20080110536A1 (en) * 2006-05-05 2008-05-15 Ganta Sudhakar R Gas generant compositions
US20080154044A1 (en) * 2006-05-05 2008-06-26 Ganta Sudhakar R Gas generant compositions
US20090008002A1 (en) * 2006-09-30 2009-01-08 Ganta Sudhakar R Gas generant compositions
US9045380B1 (en) 2007-10-31 2015-06-02 Tk Holdings Inc. Gas generating compositions

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4034645A1 (en) * 1990-10-31 1992-05-07 Fraunhofer Ges Forschung Guanidinium-5,5'-azo-tetrazolate - is stable nitrogen-rich cpd. yielding non-harmful gases upon decomposition
DE19505568A1 (en) * 1995-02-18 1996-08-22 Dynamit Nobel Ag Gas generating mixtures
SE513315C2 (en) * 1998-12-30 2000-08-21 Nexplo Bofors Ab Methods of producing gas generators for gas-powered car safety details and pyrotechnic gas generators prepared in accordance with the method

Cited By (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USB235011I5 (en) * 1971-03-16 1975-01-28
US3925086A (en) * 1971-03-16 1975-12-09 Minnesota Mining & Mfg Azotriazole and azotetrazole antifog, antistain and selective desensitizers for silver halide emulsions
EP0055547A1 (en) * 1980-12-31 1982-07-07 Morton Thiokol, Inc. Solid compositions for generating nitrogen, the generation of nitrogen therefrom and inflation of gas bags therewith
US4601344A (en) * 1983-09-29 1986-07-22 The United States Of America As Represented By The Secretary Of The Navy Pyrotechnic fire extinguishing method
US5053086A (en) * 1985-03-15 1991-10-01 The United States Of America As Represented By The Secretary Of The Navy Gas generant compositions containing energetic high nitrogen binders
US5015309A (en) * 1989-05-04 1991-05-14 Morton International, Inc. Gas generant compositions containing salts of 5-nitrobarbituric acid, salts of nitroorotic acid, or 5-nitrouracil
US5198046A (en) * 1991-03-14 1993-03-30 Fraunhofer-Gesellschaft Zur Forderung Der Angewandten Forschund E.V. Stable, nitrogen-rich composition
US5197758A (en) * 1991-10-09 1993-03-30 Morton International, Inc. Non-azide gas generant formulation, method, and apparatus
US5160386A (en) * 1991-11-04 1992-11-03 Morton International, Inc. Gas generant formulations containing poly(nitrito) metal complexes as oxidants and method
US5783773A (en) * 1992-04-13 1998-07-21 Automotive Systems Laboratory Inc. Low-residue azide-free gas generant composition
US5439251A (en) * 1992-11-30 1995-08-08 Toyo Kasei Kogyo Company Limited Method of tetrazole amine salts having improved physical properties for generating gas in airbags
US5425886A (en) * 1993-06-23 1995-06-20 The United States Of America As Represented By The Secretary Of The Navy On demand, non-halon, fire extinguishing systems
WO1995004016A1 (en) * 1993-08-02 1995-02-09 Thiokol Corporation Anhydrous tetrazole gas generant compositions and methods of preparation
WO1995004014A1 (en) * 1993-08-02 1995-02-09 Thiokol Corporation Method for preparing anhydrous tetrazole gas generant compositions
WO1995004015A1 (en) * 1993-08-02 1995-02-09 Thiokol Corporation Bitetrazoleamine gas generant compositions and methods of use
US5682014A (en) * 1993-08-02 1997-10-28 Thiokol Corporation Bitetrazoleamine gas generant compositions
US5501823A (en) * 1993-08-02 1996-03-26 Thiokol Corporation Preparation of anhydrous tetrazole gas generant compositions
US5500059A (en) * 1993-08-02 1996-03-19 Thiokol Corporation Anhydrous 5-aminotetrazole gas generant compositions and methods of preparation
US5472647A (en) * 1993-08-02 1995-12-05 Thiokol Corporation Method for preparing anhydrous tetrazole gas generant compositions
WO1995004710A1 (en) * 1993-08-04 1995-02-16 Automotive Systems Laboratory, Inc. Law residue azide-free gas generant composition
US5468866A (en) * 1994-01-04 1995-11-21 Thiokol Corporation Methods for synthesizing and processing bis-(1(2)H-tetrazol-5-yl)-amine
WO1995019341A3 (en) * 1994-01-06 1995-08-31 Thiokol Corp Process for making 5-nitrobarbituric acid and salts thereof
US5472534A (en) * 1994-01-06 1995-12-05 Thiokol Corporation Gas generant composition containing non-metallic salts of 5-nitrobarbituric acid
WO1995019342A3 (en) * 1994-01-06 1995-08-31 Thiokol Corp Gas generant composition containing non-metallic salts of 5-nitrobarbituric acid
WO1995019341A2 (en) * 1994-01-06 1995-07-20 Thiokol Corporation Process for making 5-nitrobarbituric acid and salts thereof
WO1995019342A2 (en) * 1994-01-06 1995-07-20 Thiokol Corporation Gas generant composition containing non-metallic salts of 5-nitrobarbituric acid
US5428165A (en) * 1994-01-06 1995-06-27 Thiokol Corporation Process for making 5-introbarbituric acid and salts thereof
US5451682A (en) * 1994-01-10 1995-09-19 Thiokol Corporation Method for synthesizing 5-aminotetrazole
US5516377A (en) * 1994-01-10 1996-05-14 Thiokol Corporation Gas generating compositions based on salts of 5-nitraminotetrazole
US5538567A (en) * 1994-03-18 1996-07-23 Olin Corporation Gas generating propellant
US5641938A (en) * 1995-03-03 1997-06-24 Primex Technologies, Inc. Thermally stable gas generating composition
US5514230A (en) * 1995-04-14 1996-05-07 Automotive Systems Laboratory, Inc. Nonazide gas generating compositions with a built-in catalyst
US5844164A (en) * 1996-02-23 1998-12-01 Breed Automotive Technologies, Inc. Gas generating device with specific composition
US5661261A (en) * 1996-02-23 1997-08-26 Breed Automotive Technology, Inc. Gas generating composition
US5866842A (en) * 1996-07-18 1999-02-02 Primex Technologies, Inc. Low temperature autoigniting propellant composition
US6306232B1 (en) 1996-07-29 2001-10-23 Automotive Systems Laboratory, Inc. Thermally stable nonazide automotive airbag propellants
US5872329A (en) * 1996-11-08 1999-02-16 Automotive Systems Laboratory, Inc. Nonazide gas generant compositions
US6210505B1 (en) * 1996-11-08 2001-04-03 Automotive Systems Laboratory Inc High gas yield non-azide gas generants
WO1999046222A2 (en) * 1998-03-12 1999-09-16 Automotive Systems Laboratory, Inc. High gas yield non-azide gas generants
WO1999046222A3 (en) * 1998-03-12 2000-08-03 Automotive Systems Lab High gas yield non-azide gas generants
US6645325B1 (en) * 1998-06-01 2003-11-11 Russell R. Nickel Fast-burning nitrocellulose compositions
US20040154711A1 (en) * 1998-12-30 2004-08-12 Per Sjoberg Gas-generating material for gas-actuated car safety devices
US20040231768A1 (en) * 1999-05-12 2004-11-25 Bofors Bepab Ab Composite gas-generating material for gas-actuated car safety devices
US6764562B1 (en) 1999-05-12 2004-07-20 Bofors Bepab Ab Composite gas-generating material for gas-actuated car safety devices
US20050257866A1 (en) * 2004-03-29 2005-11-24 Williams Graylon K Gas generant and manufacturing method thereof
US20100269965A1 (en) * 2004-03-29 2010-10-28 Williams Graylon K Gas generant and manufacturing method thereof
WO2006128910A1 (en) * 2005-06-02 2006-12-07 Ruag Ammotec Gmbh Pyrotechnic agent
US10968147B2 (en) 2005-06-02 2021-04-06 Ruag Ammotec Gmbh Pyrotechnic agent
US20090133787A1 (en) * 2005-06-02 2009-05-28 Ruag Ammotec Gmbh Pyrotechnic agent
JP2008542175A (en) * 2005-06-02 2008-11-27 ルアグ アモテック ゲゼルシャフト ミット ベシュレンクテル ハフツング Pyrotechnical active substance
US20080154044A1 (en) * 2006-05-05 2008-06-26 Ganta Sudhakar R Gas generant compositions
EP2038146A2 (en) * 2006-05-05 2009-03-25 TK Holdings Inc. Gas generant compositions
EP2038146A4 (en) * 2006-05-05 2009-09-30 Tk Holdings Inc Gas generant compositions
US7692024B2 (en) * 2006-05-05 2010-04-06 Tk Holdings, Inc. Gas generant compositions
US20100258220A1 (en) * 2006-05-05 2010-10-14 Ganta Sudhakar R Gas generant compositions
US20100258221A1 (en) * 2006-05-05 2010-10-14 Ganta Sudhakar R Gas generant compositions
US7847102B2 (en) 2006-05-05 2010-12-07 Tk Holdings, Inc. Gas generant compositions
US7914632B2 (en) 2006-05-05 2011-03-29 Tk Holdings, Inc. Gas generant compositions
US8088235B2 (en) 2006-05-05 2012-01-03 Tk Holdings, Inc. Gas generant compositions
US20080110536A1 (en) * 2006-05-05 2008-05-15 Ganta Sudhakar R Gas generant compositions
US20090008002A1 (en) * 2006-09-30 2009-01-08 Ganta Sudhakar R Gas generant compositions
US8002915B2 (en) 2006-09-30 2011-08-23 Tk Holdings, Inc. Gas generant compositions
US9045380B1 (en) 2007-10-31 2015-06-02 Tk Holdings Inc. Gas generating compositions

Also Published As

Publication number Publication date
GB1313619A (en) 1973-04-18
DE2004620B2 (en) 1974-12-12
CA981024A (en) 1976-01-06
DE2004620A1 (en) 1971-08-19
DE2004620C3 (en) 1975-07-17
FR2078084A5 (en) 1971-11-05

Similar Documents

Publication Publication Date Title
US3719604A (en) Pressurizing-gas-producing charges containing an aminoguanidine tetrazole and an oxygen-liberating or gas-evolving additive
US4931112A (en) Gas generating compositions containing nitrotriazalone
US6210505B1 (en) High gas yield non-azide gas generants
US5460667A (en) Gas generating agent and gas generator for automobile air bags
US5125684A (en) Extrudable gas generating propellants, method and apparatus
US2836484A (en) Aqueous metal powder explosive
KR100537348B1 (en) Lead- and barium-free igniter compounds
Shamshina et al. Catalytic ignition of ionic liquids for propellant applications
JPH09118582A (en) Charge for gas generation
US8147627B2 (en) Ignition means for propellant powders
Oxley The chemistry of explosives
US3369945A (en) Explosive composition containing an inorganic oxidizer salt,a soluble lignosulphonate,and mutual solvent therefor
CZ40699A3 (en) Thermal fuse
US2988437A (en) Cyanamide catalyst for ammonium nitrate gas generating composition
US3496040A (en) Aqueous ammonium nitrate slurry explosive compositions containing hexamethylenetetramine
US3523047A (en) Hydrazine and aluminum containing explosive compositions
US3421954A (en) Melt explosive composition having a matrix of an inorganic oxygen supplying salt
US2885277A (en) Hydrogen gas generating propellent compositions
US3269879A (en) Ammonium salt lattice with isomorphously substituted inorganic salts
US2829036A (en) Fire damp proof explosive compositions
US3397096A (en) Thickened inorganic oxidizer salt explosive slurry sensitized with a soluble polyflavonoid
US3028273A (en) Catalyst for nh4no3 combustion
Fronabarger et al. Alternatives to existing primary explosives
JP5019550B2 (en) Double salt of ammonium nitrate, process for producing the same, and gas generating agent using the same
JP3132169B2 (en) Gas generating agent