USRE41557E1 - Labile bromine fire suppressants - Google Patents
Labile bromine fire suppressants Download PDFInfo
- Publication number
- USRE41557E1 USRE41557E1 US12/263,054 US26305408A USRE41557E US RE41557 E1 USRE41557 E1 US RE41557E1 US 26305408 A US26305408 A US 26305408A US RE41557 E USRE41557 E US RE41557E
- Authority
- US
- United States
- Prior art keywords
- composition
- propellant
- fire
- liberated
- bromine atoms
- 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
Links
Classifications
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/0028—Liquid extinguishing substances
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/0007—Solid extinguishing substances
- A62D1/0014—Powders; Granules
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/0092—Gaseous extinguishing substances, e.g. liquefied gases, carbon dioxide snow
Definitions
- the present invention generally relates to prevention and extinguishment of fires of combustible materials by utilizing a composition of matter group which is highly efficient and environmentally friendly. More particularly, the invention relates to prevention and extinguishment of fires of combustible materials by using a group of fire suppressants having labile bonds between bromine atoms and atoms other than carbon.
- Fire suppression by halogenated alkanes is well-established in both the scientific literature and commercial practice as taught, for example, in R. G. Gann ed., Halogenated Fire Suppressants, ACS Symposium Series 16 (American Chemical Society, Washington, D.C.) 1975.
- the two most widely used halogenated suppressants are Halon 1301 (CF 3 Br) and Halon 1211 (CF 2 ClBr). These compounds are very stable, so they survive long enough in the troposphere to be gradually transported to the stratosphere, where they are photolyzed by solar ultraviolet radiation to produce free radicals that catalyze ozone depletion as taught, for example, in J. G. Anderson, D. W. Toohey, and W. F. Brune, Science, 251, 39 (1991).
- compositions of matter having labile bromine atoms bound to atoms other than carbon have been discovered to have improved fire suppressant properties and to be environmentally friendly.
- Compounds which release bromine atoms and are commonly used as brominating agents in organic synthesis such as phosphorous tribromide (PBr 3 ), thionyl bromide (SOBr 2 ), boron tribromide (BBr 3 ), and the like are very efficient at extinguishing fires. Moreover, they hydrolyze or oxidize rapidly in the troposphere and consequently they have no stratospheric ozone depletion potential.
- SiBr 4 silicon tetrabromide
- TiBr 4 titanium tetrabromide
- IBr iodine bromide
- POBr 3 phosphorous oxybromide
- bromine trifluoride BrF 3
- bromine pentafluoride BrF 5
- N-bromosuccinimide C 4 H 4 O 2 NBr
- non-labile bromine compositions are found in such high-melting, ionically bound salts as lithium bromide (LiBr, m.p. 547° C.), calcium bromide (CaBr 2 , m.p. 730° C.), or chromous bromide (CrBr 2 , m.p. 842° C.), and other bromine-containing compositions that are thermally and oxidatively stable according to criteria familiar to people practiced in the art of synthetic chemistry.
- lithium bromide LiBr, m.p. 547° C.
- CaBr 2 calcium bromide
- CrBr 2 chromous bromide
- equipment for delivering the composition incorporates such factors as specific geometry, gas flow, and flame conditions.
- a method of delivery of a composition having one or more liquid compounds of the aforesaid class of fires suppressants may employ a nonflammable, pressurized gas to propel the composition through a nozzle to the flame.
- Another method of delivery of liquid compositions may employ a deflagrating solid, gas-generating cartridge, such as is found in automotive airbags, to propel a mist of liquid to the flame.
- a third method for delivery of liquid compositions may employ a pressurized liquid propellant such as liquid carbon dioxide or liquid argon to atomize and direct a mist of suppressant onto the flame.
- a pressurized liquid propellant such as liquid carbon dioxide or liquid argon
- Other methods for propelling powders or slurries of solid materials of the aforesaid class may employ a deflagrating solid gas generating cartridge and a wider nozzle such as would be used for an ordinary shotgun cartridge.
- Other methods for propelling gaseous materials of the aforesaid class may employ mixtures with pressurized inert propellants to aid transport of suppressant to the flame.
- the primary advantage of the use of the class of fire suppressants of this discovery is to extinguish fires more efficiently with smaller volumes and masses of extinguishant than existing fire suppressants, without depleting the stratospheric ozone layer.
- PBr 3 , POBr 3 , SOBr 2 , BBr 3 , and the like react rapidly with water vapor or liquid to produce mild acids which precipitate with normal rain and are ultimately neutralized in soils.
- the short lifetimes of these materials also reduce toxicity of the suppressants since their simple acid decomposition products pose no chronic risk to pH buffered, living organisms.
- the effectiveness of the class of suppressants described herein is a result of the relative ease with which bromine atoms are liberated in a flame environment.
- Halons 1301 and 1211 also liberate bromine atoms in a flame; however, the strength of the C—Br bond in these materials requires higher temperatures or longer interaction times than the compositions of matter described herein.
- the stability of the Halons against oxidation or hydrolysis in the troposphere is one indication of the stability of the C—Br bond.
- the compositions of matter described herein are not stable in the presence of water, oxygen, or heat, liberating bromine atoms under these conditions and thereby providing a catalyst for flame suppression.
- liquid SOBr 2 is introduced as an air-pressurized mist into a 500,000 Btu/hr fire resulting from kerosene flowing at a rate of 4 grams per second through a nozzle with cross-flowing compressed air to atomize the liquid into a fine mist.
- the fire is contained in a flame holder whose volume is approximately 8 liters and is further blown by an atmospheric cross-wind of 40 miles per hour.
- the fire is reproducibly and irreversibly extinguished with less than one gram of SOBr 2 in less than 0.2 seconds as confirmed by videotape records of the experiments.
- the same fire is not reproducibly suppressed with aliquots of 25 grams of CF 3 Br added to the same location.
- PBr 3 0.2 cubic centimeters of PBr 3 is mixed with 0.7 cubic centimeters of liquid carbon dioxide.
- the liquid CO 2 propels the PBr 3 through a valve and into the flame zone, generated as herein above described, as it is opened, irreversibly and completely extinguishing the flame in the presence of flowing fuel, air, and hot surfaces.
- Halon 1301 Extinguishment of a similar fire, with a hydrocarbon fuel burn rate of 12 grams per second, by Halon 1301 is taught by Alvarez in chapter 3 of Gann (ibid.) to require between 90 and 130 grams per second of CF 3 Br for suppression.
- Another example of a gasoline fire with similar heat output is taught by Ford in chapter 1 of Gann (ibid.) to require between 500 and 1500 grams of Halon 1301 for suppression.
- Another fire, in which 10 grams per second of jet fuel are burned in fast-flowing air at the Air Force Flight Dynamics Laboratory Engine Nacelle test facility (Wright-Patterson AFB, OH) requires between one and three kilograms of Halon 1301 for reproducible suppression.
- the quantity of Halon 1301 required to suppress a similar fire is between 100 and 1000 times greater than that required of the compositions of matter described herein above, of which SOBr 2 and PBr 3 are specific embodiments.
- the labile bromine atoms and high proportion of bromine in the composition of matter listed in Table I provide a more efficient fire suppression formulation than the Halons, which typically have less bromine by weight (Halon 1301 and 1211 are 54% and 48% Br, respectively) and lesser proclivity for liberating bromine atoms when thermally or chemically activated in a combustion environment.
- Methods for dispersing gas, liquid, or solid suppressants require designs based upon such factors as specific geometry of the locus of the fire, flow properties of the fire suppressants, and flame conditions of the fire. For example, fine mists of liquid are transported by fluid-dynamical drag forces along flow streamlines in the nacelle of an aircraft engine. The mists vaporize in hot zones, liberating bromine atoms by pyrolysis in precisely the regions where the heat released by combustion is most intense. Inasmuch as the drag coefficient is inversely proportional to the droplet diameter, as is known to people practiced in the art of fluid dynamics, there is a range of aerosol size distributions which most effectively deliver specific suppressants to specific fires.
- Dispersing methods designed for suppressing fire in the nacelle of a jet engine differ from dispersing methods designed for suppressing fire in the engine compartment of a motor vehicle, the flu of a chimney, or the gas-handling manifold of a semiconductor processing clean-room.
Abstract
A class of fire suppressant compounds which have labile bromine atoms bound to atoms other than carbon have been discovered to be more effective at suppressing fires than Halon 1211 and Halon 1301. Moreover, this class of fire suppressant compounds hydrolyze or oxidize rapidly in the troposphere and as a consequence thereof, they have minimal ozone depletion potential.
Description
More than one divisional reissue application has been filed for the reissue of U.S. Pat. No. 5,626,786. The reissue applications are application Ser. No. 10/893,705 now RE40,651 E, application Ser. No. 12/263,122 pending, and the present application Ser. No. 12/263,054.
This invention was made with support by the U.S. Government. The Government may have certain rights in this invention.
1. Field of the Invention
The present invention generally relates to prevention and extinguishment of fires of combustible materials by utilizing a composition of matter group which is highly efficient and environmentally friendly. More particularly, the invention relates to prevention and extinguishment of fires of combustible materials by using a group of fire suppressants having labile bonds between bromine atoms and atoms other than carbon.
2. Description of the Prior Art
Fire suppression by halogenated alkanes is well-established in both the scientific literature and commercial practice as taught, for example, in R. G. Gann ed., Halogenated Fire Suppressants, ACS Symposium Series 16 (American Chemical Society, Washington, D.C.) 1975. The two most widely used halogenated suppressants are Halon 1301 (CF3Br) and Halon 1211 (CF2ClBr). These compounds are very stable, so they survive long enough in the troposphere to be gradually transported to the stratosphere, where they are photolyzed by solar ultraviolet radiation to produce free radicals that catalyze ozone depletion as taught, for example, in J. G. Anderson, D. W. Toohey, and W. F. Brune, Science, 251, 39 (1991). Production of these materials has therefore been internationally prohibited after January, 1994 by the Montreal Protocol on Substances that Deplete the Ozone Layer. The problem is therefore to find fire suppression materials and methods which are at least as effective as Halon 1301 and Halon 1211 but which do not deplete the ozone layer.
Representative of the prior art directed to the use of fluorocarbons which have no chlorine or bromine is U.S. Pat. No. 5,236,611 (Shiflet). These fluorocarbons are slowly transported into the stratosphere, but the catalytic efficiency of fluorine is very much smaller than that of chlorine, bromine, or iodine.
Representative of the prior art directed to the use of hydrogenated halocarbons, which are less stable than Halon 1301 or Halon 1211 in the troposphere, are U.S. Pat. Nos. 5,084,190 (Fernandez), 5,135,054 (Nimitz et al.); 5,093,013 (Sprague); and 5,080,177 (Robin et al.). It is well known that Halons containing chlorine or bromine will suppress fires in smaller quantities than those which contain only fluorine. However, it is understood by people practiced in the art of combustion that the principal source of heat release in hydrocarbon combustion is oxidation of hydrogen atoms to form water vapor. Thus hydrogenated halocarbons are expected to act chemically both as fuels and as fire suppressants.
In accordance with the teachings of the present invention compositions of matter having labile bromine atoms bound to atoms other than carbon have been discovered to have improved fire suppressant properties and to be environmentally friendly. Compounds which release bromine atoms and are commonly used as brominating agents in organic synthesis such as phosphorous tribromide (PBr3), thionyl bromide (SOBr2), boron tribromide (BBr3), and the like are very efficient at extinguishing fires. Moreover, they hydrolyze or oxidize rapidly in the troposphere and consequently they have no stratospheric ozone depletion potential.
Additionally included in this class of fire suppressant compounds of labile bromine atoms bound to atoms other than carbon are silicon tetrabromide (SiBr4), titanium tetrabromide (TiBr4), iodine bromide (IBr), phosphorous oxybromide (POBr3), bromine trifluoride (BrF3), bromine pentafluoride (BrF5), N-bromosuccinimide (C4H4O2NBr) {the bromine is bound to nitrogen, not carbon}, nitrosyl bromide (NOBr), chlorine bromide (ClBr), and cuprous bromide (CuBr). These compounds are used as brominating agents in chemical synthesis as taught, for example, in the Merck Index, ninth edition, (Merck & Co., Rahway, N.J., 1976) or suffer thermal decomposition with liberation of bromine at temperatures less than 200 degrees centigrade.
Examples of non-labile bromine compositions are found in such high-melting, ionically bound salts as lithium bromide (LiBr, m.p. 547° C.), calcium bromide (CaBr2, m.p. 730° C.), or chromous bromide (CrBr2, m.p. 842° C.), and other bromine-containing compositions that are thermally and oxidatively stable according to criteria familiar to people practiced in the art of synthetic chemistry.
In order to extinguish fires with a composition having one or more compounds of the aforesaid class of fire suppressants, equipment for delivering the composition incorporates such factors as specific geometry, gas flow, and flame conditions. A method of delivery of a composition having one or more liquid compounds of the aforesaid class of fires suppressants may employ a nonflammable, pressurized gas to propel the composition through a nozzle to the flame. Another method of delivery of liquid compositions may employ a deflagrating solid, gas-generating cartridge, such as is found in automotive airbags, to propel a mist of liquid to the flame. A third method for delivery of liquid compositions may employ a pressurized liquid propellant such as liquid carbon dioxide or liquid argon to atomize and direct a mist of suppressant onto the flame. Other methods for propelling powders or slurries of solid materials of the aforesaid class may employ a deflagrating solid gas generating cartridge and a wider nozzle such as would be used for an ordinary shotgun cartridge. Other methods for propelling gaseous materials of the aforesaid class may employ mixtures with pressurized inert propellants to aid transport of suppressant to the flame.
The primary advantage of the use of the class of fire suppressants of this discovery is to extinguish fires more efficiently with smaller volumes and masses of extinguishant than existing fire suppressants, without depleting the stratospheric ozone layer. PBr3, POBr3, SOBr2, BBr3, and the like react rapidly with water vapor or liquid to produce mild acids which precipitate with normal rain and are ultimately neutralized in soils. The short lifetimes of these materials also reduce toxicity of the suppressants since their simple acid decomposition products pose no chronic risk to pH buffered, living organisms.
These and other advantages and attainments of the present invention will become apparent to those skilled in the art upon a reading of the detailed description wherein there are described several embodiments of the invention.
In accordance with the teachings of the present invention a class of fire suppressants which have labile bromine atoms bound to atoms other than carbon are shown in Table I. These compounds are more effective at suppressing fire than Halon 1301 or Halon 1211 and have no ozone depletion potential.
The effectiveness of the class of suppressants described herein is a result of the relative ease with which bromine atoms are liberated in a flame environment. Halons 1301 and 1211 also liberate bromine atoms in a flame; however, the strength of the C—Br bond in these materials requires higher temperatures or longer interaction times than the compositions of matter described herein. The stability of the Halons against oxidation or hydrolysis in the troposphere is one indication of the stability of the C—Br bond. The compositions of matter described herein are not stable in the presence of water, oxygen, or heat, liberating bromine atoms under these conditions and thereby providing a catalyst for flame suppression.
Another indication of the stability of the C—Br bond is the measurement of its bond dissociation energy of 68 kilocalories per mole as taught by A. H. Sehon and M. Szwarc (Proceedings of the Royal Society (London), page 110, [1951]). This energy is larger than the bond energy of typical P—Br bonds (63 kcal/mole), I—Br bonds (43 kcal/mole), or S—Br bonds (52 kcal/mole) as taught by Streitweiser and Heathcock, Introduction to Organic Chemistry, (Macmillan:NY), 1976 and Cotton and Wilkinson, Advanced Inorganic Chemistry, (3rd ed. Wiley:NY), 1972. As is known to people practiced in the art of chemistry the interpretation of bond dissociation energies involves approximations based on the nature of the full molecular fragments (XYn) from which bromine is liberated according to the reaction:
YnX—Br→YnX+Br.
Thus lower average bond energies indicate the possibility of labile bonds in a group of materials, but further experimentation with specific materials is required to establish the lability of the bond compared with Halons.
YnX—Br→YnX+Br.
Thus lower average bond energies indicate the possibility of labile bonds in a group of materials, but further experimentation with specific materials is required to establish the lability of the bond compared with Halons.
| TABLE I | |||||
| Composition | Phase | % Br | Comments | ||
| PBr3 | liquid | 88 | brominating agent | ||
| POBr3 | liquid | 83 | brominating agent | ||
| SOBr2 | liquid | 77 | brominating agent | ||
| BrF3 | liquid | 58 | reactive solvent | ||
| BrF5 | liquid | 46 | reactive solvent | ||
| PBr5 | solid | 91 | brominating agent | ||
| TiBr4 | solid | 87 | reacts with water | ||
| SiBr4 | liquid | 92 | reacts with water | ||
| IBr | solid | 39 | decomposes at 116° C. | ||
| CuBr | solid | 29 | brominating agent | ||
| NOBr | gas | 73 | brominating agent | ||
| B2F | gas | 81 | boils at −20° C. | ||
| C6H4O2NBr | solid | 44.9 | decomposes at 170° C. | ||
| BBr3 | liquid | 96 | boils at 90° C. | ||
| BrCl | gas | 70 | decomposes at 10° C. | ||
In one embodiment of the invention liquid SOBr2 is introduced as an air-pressurized mist into a 500,000 Btu/hr fire resulting from kerosene flowing at a rate of 4 grams per second through a nozzle with cross-flowing compressed air to atomize the liquid into a fine mist. The fire is contained in a flame holder whose volume is approximately 8 liters and is further blown by an atmospheric cross-wind of 40 miles per hour. The fire is reproducibly and irreversibly extinguished with less than one gram of SOBr2 in less than 0.2 seconds as confirmed by videotape records of the experiments. The same fire is not reproducibly suppressed with aliquots of 25 grams of CF3Br added to the same location.
In another embodiment of the invention 0.2 cubic centimeters of PBr3 is mixed with 0.7 cubic centimeters of liquid carbon dioxide. The liquid CO2 propels the PBr3 through a valve and into the flame zone, generated as herein above described, as it is opened, irreversibly and completely extinguishing the flame in the presence of flowing fuel, air, and hot surfaces.
Extinguishment of a similar fire, with a hydrocarbon fuel burn rate of 12 grams per second, by Halon 1301 is taught by Alvarez in chapter 3 of Gann (ibid.) to require between 90 and 130 grams per second of CF3Br for suppression. Another example of a gasoline fire with similar heat output is taught by Ford in chapter 1 of Gann (ibid.) to require between 500 and 1500 grams of Halon 1301 for suppression. Another fire, in which 10 grams per second of jet fuel are burned in fast-flowing air at the Air Force Flight Dynamics Laboratory Engine Nacelle test facility (Wright-Patterson AFB, OH) requires between one and three kilograms of Halon 1301 for reproducible suppression. In each of these examples the quantity of Halon 1301 required to suppress a similar fire is between 100 and 1000 times greater than that required of the compositions of matter described herein above, of which SOBr2 and PBr3 are specific embodiments.
The labile bromine atoms and high proportion of bromine in the composition of matter listed in Table I provide a more efficient fire suppression formulation than the Halons, which typically have less bromine by weight (Halon 1301 and 1211 are 54% and 48% Br, respectively) and lesser proclivity for liberating bromine atoms when thermally or chemically activated in a combustion environment.
Methods for dispersing gas, liquid, or solid suppressants require designs based upon such factors as specific geometry of the locus of the fire, flow properties of the fire suppressants, and flame conditions of the fire. For example, fine mists of liquid are transported by fluid-dynamical drag forces along flow streamlines in the nacelle of an aircraft engine. The mists vaporize in hot zones, liberating bromine atoms by pyrolysis in precisely the regions where the heat released by combustion is most intense. Inasmuch as the drag coefficient is inversely proportional to the droplet diameter, as is known to people practiced in the art of fluid dynamics, there is a range of aerosol size distributions which most effectively deliver specific suppressants to specific fires. Another such factor for a gaseous composition is the mixing of suppressant flow with turbulent flames in a well-ventilated fire, which is affected by the delivery pressure, the nozzle contour and orientation, the mass-flow rate of the suppressant, and the fluid dynamical properties of the fire. Dispersing methods designed for suppressing fire in the nacelle of a jet engine differ from dispersing methods designed for suppressing fire in the engine compartment of a motor vehicle, the flu of a chimney, or the gas-handling manifold of a semiconductor processing clean-room.
Methods for preventing and extinguishing fires of jet fuel using a composition of matter class which is highly efficient and environmentally friendly is also disclosed by the present inventors in Final Technical Report FR-4021 (US Air Force Phase I SBIR Contract F33615-94-C-5005, November 1994).
Although preferred embodiments of the invention have been described, it will be understood that within the scope of this invention various changes may be made in the amount of fire suppressant, the composition of a fire suppressant mixture, and the method for dispersing fire suppressants which is generally stated consist of a class of fire suppressants and methods of dispersing such fire suppressants capable of carrying out the objects set forth as disclosed in the appended claims.
Claims (48)
1. A fire suppressant composition consisting essentially of at least one brominated, non-carbon compound selected from the group consisting of PBr3, POBr3, SOBr2, BrF3, BrF5, PBr5, TiBr4, SiBr4, IBr, CuBr, NOBr, BrF, and BBr3, which is combined with a propellant such that the ozone depletion potential of the composition is less than 0.1.
2. The fire suppressant composition of claim 1 wherein ozone depletion potential is defined on a scale where the ozone depletion caused by CFCl3 is 1.0.
3. A fire suppressant composition consisting of at least one labile brominated compound selected from the group consisting of PBr3, POBr3, SOBr2, BrF3, BrF5, TiBr4, SiBr4, IBr, CuBr, NOBr, BrF, BBr3, and BrCl, which is combined with a propellant selected from the group consisting of CO2, N2, compressed air, and HCFC-123 (CF3CCl2H).
4. The fire suppressant composition of claim 3 wherein ozone depletion potential of the propellant equals 0.016.
5. A fire suppressant composition consisting essentially of: at least one brominated, non-carbon compound in a liquid state selected from the group consisting of CuBr, IBr, and BrCl; and a propellant combined with the compound for propelling the composition such that sufficient bromine atoms are liberated from the composition to suppress a fire, wherein the composition has no ozone depletion potential.
6. The composition of claim 5 , wherein the propellant is selected from the group consisting of CO2 , N 2 , and compressed air.
7. The composition of claim 5 wherein said brominated compound is CuBr.
8. The composition of claim 5 wherein said brominated compound is IBr.
9. The composition of claim 5 wherein said brominated compound is BrCl.
10. The composition of claim 5 wherein said brominated compound is CuBr and the propellant is nonflammable.
11. The composition of claim 5 wherein said brominated compound is IBr and the propellant is nonflammable.
12. The composition of claim 5 wherein said brominated compound is BrCl and the propellant is nonflammable.
13. The composition of claim 7 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of oxygen.
14. The composition of claim 13 wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
15. The composition of claim 7 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of heat.
16. The composition of claim 15 wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
17. The composition of claim 7 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of water.
18. The composition of claim 17 wherein said wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
19. The composition of claim 8 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of oxygen.
20. The composition of claim 19 wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
21. The composition of claim 8 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of heat.
22. The composition of claim 21 wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
23. The composition of claim 8 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of water.
24. The composition of claim 23 wherein said wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
25. The composition of claim 9 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of oxygen.
26. The composition of claim 25 wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
27. The composition of claim 9 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of heat.
28. The composition of claim 27 wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
29. The composition of claim 9 wherein said brominated compound is not stable in, and said sufficient bromine atoms are liberated in, the presence of water.
30. The composition of claim 29 wherein said wherein said liberated bromine atoms are sufficient to catalytically suppress the fire.
31. The composition of claim 7 wherein the propellant is selected from the group consisting of a non-flammable, pressurized gas; a deflagrating, solid, gas-generating cartridge; and a pressurized liquid.
32. The composition of claim 8 wherein the propellant is selected from the group consisting of a non-flammable, pressurized gas; a deflagrating, solid, gas-generating cartridge; and a pressurized liquid.
33. The composition of claim 9 wherein the propellant is selected from the group consisting of a non-flammable, pressurized gas; a deflagrating, solid, gas-generating cartridge; and a pressurized liquid.
34. A fire suppressant composition consisting essentially of CuBr in a liquid state and a propellant combined with the CuBr for propelling the composition to catalytically suppress a fire, wherein the composition has no ozone depletion potential.
35. The composition of claim 34 , wherein the propellant is selected from the group consisting of CO2 , N 2 , and compressed air.
36. The composition of claim 34 wherein the propellant is nonflammable.
37. The composition of claim 34 wherein the CuBr is not stable in the presence of at least one of oxygen, heat, and water.
38. The composition of claim 34 wherein the propellant is selected from the group consisting of a non-flammable, pressurized gas; a deflagrating, solid, gas-generating cartridge; and a pressurized liquid.
39. A fire suppressant composition consisting essentially of IBr in a liquid stage and a propellant combined with the IBr for propelling the composition to catalytically suppress a fire, wherein the composition has no ozone depletion potential.
40. The composition of claim 39 , wherein the propellant is selected from the group consisting of CO2 , N 2 , and compressed air.
41. The composition of claim 39 wherein the propellant is nonflammable.
42. The composition of claim 39 wherein the CuBr is not stable in the presence of at least one of oxygen, heat, and water.
43. The composition of claim 39 wherein the propellant is selected from the group consisting of a non-flammable, pressurized gas; a deflagrating, solid, gas-generating cartridge; and a pressurized liquid.
44. A fire suppressant composition consisting essentially of BrCl in a liquid state and a propellant combined with the BrCl for propelling the composition to catalytically suppress a fire, wherein the composition has no ozone depletion potential.
45. The composition of claim 44 , wherein the propellant is selected from the group consisting of CO2 , N 2 , and compressed air.
46. The composition of claim 44 wherein the propellant is nonflammable.
47. The composition of claim 44 wherein the CuBr is not stable in the presence of at least one of oxygen, heat, and water.
48. The composition of claim 44 wherein the propellant is selected from the group consisting of a non-flammable, pressurized gas; a deflagrating, solid, gas-generating cartridge; and a pressurized liquid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/263,054 USRE41557E1 (en) | 1995-04-17 | 2008-10-31 | Labile bromine fire suppressants |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/423,209 US5626786A (en) | 1995-04-17 | 1995-04-17 | Labile bromine fire suppressants |
| US12/263,054 USRE41557E1 (en) | 1995-04-17 | 2008-10-31 | Labile bromine fire suppressants |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/423,209 Reissue US5626786A (en) | 1995-04-17 | 1995-04-17 | Labile bromine fire suppressants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE41557E1 true USRE41557E1 (en) | 2010-08-24 |
Family
ID=23678043
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/423,209 Ceased US5626786A (en) | 1995-04-17 | 1995-04-17 | Labile bromine fire suppressants |
| US10/893,705 Expired - Lifetime USRE40651E1 (en) | 1995-04-17 | 2004-07-16 | Labile bromine fire suppressants |
| US12/263,122 Expired - Lifetime USRE41558E1 (en) | 1995-04-17 | 2008-10-31 | Labile bromine fire suppressants |
| US12/263,054 Expired - Lifetime USRE41557E1 (en) | 1995-04-17 | 2008-10-31 | Labile bromine fire suppressants |
Family Applications Before (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/423,209 Ceased US5626786A (en) | 1995-04-17 | 1995-04-17 | Labile bromine fire suppressants |
| US10/893,705 Expired - Lifetime USRE40651E1 (en) | 1995-04-17 | 2004-07-16 | Labile bromine fire suppressants |
| US12/263,122 Expired - Lifetime USRE41558E1 (en) | 1995-04-17 | 2008-10-31 | Labile bromine fire suppressants |
Country Status (1)
| Country | Link |
|---|---|
| US (4) | US5626786A (en) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5626786A (en) * | 1995-04-17 | 1997-05-06 | Huntington; John H. | Labile bromine fire suppressants |
| US6082464A (en) * | 1997-07-22 | 2000-07-04 | Primex Technologies, Inc. | Dual stage fire extinguisher |
| DE69838485T2 (en) | 1997-10-09 | 2008-06-26 | Emory University | METHOD AND DEVICE FOR THE TRANSDERMAL ADMINISTRATION OF LITHIUM |
| US5861106A (en) * | 1997-11-13 | 1999-01-19 | Universal Propulsion Company, Inc. | Compositions and methods for suppressing flame |
| US6513602B1 (en) * | 2000-09-13 | 2003-02-04 | Universal Propolsion Company | Gas generating device |
| DE60142570D1 (en) | 2000-09-13 | 2010-08-26 | Goodrich Corp | GAS GENERATION DEVICE |
| US7758633B2 (en) * | 2004-04-12 | 2010-07-20 | Boston Scientific Scimed, Inc. | Varied diameter vascular graft |
| JP5389359B2 (en) * | 2005-01-12 | 2014-01-15 | エクリプス エアロスペース，インコーポレイテッド | Fire suppression system |
| US20070007019A1 (en) * | 2005-06-17 | 2007-01-11 | Aerojet-General Corporation | Hybrid fire extinguisher for extended suppression times |
| US10294658B2 (en) | 2008-12-23 | 2019-05-21 | Xoma (Us) Llc | Flexible manufacturing system |
| US9795957B2 (en) * | 2009-08-16 | 2017-10-24 | G-Con Manufacturing, Inc. | Modular, self-contained, mobile clean room |
| JP5879264B2 (en) | 2009-08-16 | 2016-03-08 | ジー−コン マニュファクチャリング インク． | Modular, independent, mobile clean room |
| WO2012080172A2 (en) * | 2010-12-16 | 2012-06-21 | Air Products And Chemicals, Inc. | A process for filling a gas storage container |
| US8920668B2 (en) * | 2012-03-16 | 2014-12-30 | Meggitt Safety Systems Inc. | Fire suppressing materials and systems and methods of use |
| US9713732B2 (en) | 2012-03-16 | 2017-07-25 | Meggitt Safety Systems, Inc. | Fire suppressing materials and systems and methods of use |
| US9034202B2 (en) | 2012-03-16 | 2015-05-19 | Meggitt Safety Systems Inc. | Fire suppressing materials and systems and methods of use |
| EP2934775B1 (en) * | 2012-12-18 | 2021-03-17 | Seastar Chemicals Inc. | Process and method for in-situ dry cleaning of thin film deposition reactors and thin film layers |
| ES2884110T3 (en) * | 2017-09-12 | 2021-12-10 | Milano Politecnico | CO2-based mixtures as a working fluid in thermodynamic cycles |
| US11624182B2 (en) | 2019-08-15 | 2023-04-11 | G-Con Manufacturing, Inc. | Removable panel roof for modular, self-contained, mobile clean room |
| US11492795B2 (en) | 2020-08-31 | 2022-11-08 | G-Con Manufacturing, Inc. | Ballroom-style cleanroom assembled from modular buildings |
Citations (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US955316A (en) * | 1907-07-26 | 1910-04-19 | Minimax Cons Ltd | Process of extinguishing burning benzin, &c. |
| US2732410A (en) * | 1956-01-24 | Process for preparing tetrafluoro | ||
| US2791490A (en) * | 1952-04-29 | 1957-05-07 | Du Pont | Method and means for commingling and reacting fluid substances |
| US2918125A (en) * | 1955-05-09 | 1959-12-22 | William G Sweetman | Chemical cutting method and apparatus |
| US3076507A (en) * | 1958-05-16 | 1963-02-05 | William G Sweetman | Chemical cutting method and apparatus for use in wells |
| US3266674A (en) * | 1964-08-24 | 1966-08-16 | Richard L Smith | Thermo-shave dispensing and reusable unit |
| US3372208A (en) * | 1964-03-20 | 1968-03-05 | Dow Chemical Co | Flame resistant epoxy resins containing phosphorus and a halogen |
| US3479286A (en) * | 1965-09-22 | 1969-11-18 | Montedison Spa | Flame-extinguishing compositions |
| US3637022A (en) * | 1969-10-30 | 1972-01-25 | Marathon Oil Co | Use of high water content oil-external micellar solutions for extinguishing fires |
| US3657030A (en) * | 1970-07-31 | 1972-04-18 | Bell Telephone Labor Inc | Technique for masking silicon nitride during phosphoric acid etching |
| US3663283A (en) * | 1969-10-02 | 1972-05-16 | Richard A Hebert | Process and apparatus for the production of finely-divided metal oxides |
| US3812239A (en) * | 1969-09-25 | 1974-05-21 | Ppg Industries Inc | Preparation of submicron titanium carbide |
| US3903037A (en) * | 1972-08-31 | 1975-09-02 | Monsanto Co | Low melt viscosity self-extinguishing polymeric polyblend |
| US3959741A (en) * | 1975-06-09 | 1976-05-25 | United Technologies Corporation | Interhalogen based combustion-driven laser which provides continuous wave output lasing from dual species |
| US3985689A (en) * | 1973-05-25 | 1976-10-12 | Minnesota Mining And Manufacturing Company | Sorbent foam material |
| US4022872A (en) * | 1975-11-12 | 1977-05-10 | Ppg Industries, Inc. | Process for preparing finely-divided refractory powders |
| US4043950A (en) * | 1973-08-27 | 1977-08-23 | Wilmsen Hans | Process for the manufacture of plastic foams and flame-proofing foams characterized by the use of a carrier foam |
| US4048290A (en) * | 1976-01-28 | 1977-09-13 | Cabot Corporation | Process for the production of finely-divided metal and metalloid oxides |
| US4125161A (en) * | 1977-04-18 | 1978-11-14 | Weatherford/Dmc, Inc. | Chemical cutting apparatus and method for use in wells |
| US4129513A (en) * | 1974-07-09 | 1978-12-12 | The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Electric field responsive fluids |
| US4241042A (en) * | 1978-06-19 | 1980-12-23 | Montedison S.P.A. | Spherical titanium dioxide particles and process of manufacture |
| JPS569230A (en) * | 1979-06-28 | 1981-01-30 | Nippon Telegr & Teleph Corp <Ntt> | Manufacture of high purity quartz glass pipe |
| US4292290A (en) * | 1980-04-16 | 1981-09-29 | Cabot Corporation | Process for the production of finely-divided metal and metalloid oxides |
| SU981338A1 (en) * | 1981-06-29 | 1982-12-15 | Всесоюзный научно-исследовательский институт противопожарной обороны МВД СССР | Combustion inhibitor |
| US4397977A (en) * | 1979-08-23 | 1983-08-09 | Pennwalt Corporation | Tetrahalophthalates as flame retardant plasticizers for halogenated resins |
| US4406797A (en) * | 1981-11-03 | 1983-09-27 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Fire extinguishant materials |
| US4415029A (en) * | 1981-07-23 | 1983-11-15 | Gearhart Industries, Inc. | Downhole well tool and anchoring assembly |
| US4428430A (en) * | 1981-01-13 | 1984-01-31 | Gearhart Industries, Inc. | Chemical method and apparatus for perforating drill collars |
| US4481119A (en) * | 1983-03-11 | 1984-11-06 | The United States Of America As Represented By The Secretary Of The Navy | Compositions for extinguishing titanium fires |
| US4494601A (en) * | 1981-09-14 | 1985-01-22 | Gearhart Industries, Inc. | Downhole chemical cutting tool |
| US4619318A (en) * | 1984-09-27 | 1986-10-28 | Gearhart Industries, Inc. | Chemical cutting method and apparatus |
| US4819728A (en) * | 1987-09-01 | 1989-04-11 | Lafitte Louis D | Pressure relief system for down hole chemical cutters |
| US4822513A (en) * | 1984-11-12 | 1989-04-18 | Diversey Corporation | Cleaning/disinfecting process and composition |
| US4889187A (en) * | 1988-04-25 | 1989-12-26 | Jamie Bryant Terrell | Multi-run chemical cutter and method |
| US4971146A (en) * | 1988-11-23 | 1990-11-20 | Terrell Jamie B | Downhole chemical cutting tool |
| US5017525A (en) * | 1987-03-25 | 1991-05-21 | Imperial Chemical Industries Plc | Production of ceramic materials and of precursor therefor |
| US5055208A (en) * | 1991-01-02 | 1991-10-08 | Powsus, Inc. | Fire extinguishing compositions |
| US5080177A (en) * | 1990-07-26 | 1992-01-14 | Great Lakes Chemical Corporation | Fire extinguishing methods utilizing 1-bromo-1,1,2,2-tetra-fluoroethane |
| US5082575A (en) * | 1987-09-29 | 1992-01-21 | Shin-Etsu Handotai Company, Ltd. | Method for fire-extinguishment on hardly extinguishable burning materials |
| US5084190A (en) * | 1989-11-14 | 1992-01-28 | E. I. Du Pont De Nemours And Company | Fire extinguishing composition and process |
| US5093013A (en) * | 1989-12-11 | 1992-03-03 | Halocarbon Products Corporation | Ozone friendly fire-extinguishing agents |
| US5120689A (en) * | 1986-03-27 | 1992-06-09 | Imperial Chemical Industries Plc | Coked product containing domains of oxides |
| US5135054A (en) * | 1990-10-05 | 1992-08-04 | University Of New Mexico | Fire extinguishing agents for flooding applications |
| US5165916A (en) * | 1989-10-02 | 1992-11-24 | Phillips Petroleum Company | Method for producing carbide products |
| US5192714A (en) * | 1990-02-14 | 1993-03-09 | Kabushiki Kaisha Toshiba | Method of manufacturing a multilayered metallization structure in which the conductive layer and insulating layer are selectively deposited |
| US5219474A (en) * | 1989-11-17 | 1993-06-15 | Korea Institute Of Science And Technology | Liquid fire extinguishing composition |
| US5235000A (en) * | 1990-12-10 | 1993-08-10 | Ethyl Corporation | Preparation, storage, and usage of bromine chloride |
| US5236611A (en) * | 1991-10-28 | 1993-08-17 | E. I. Du Pont De Nemours And Company | Mixtures of perfluoropropane and trifluoroethane |
| WO1993015794A1 (en) * | 1992-02-05 | 1993-08-19 | Ab Bejaro-Product | Gas-liquid mixture as well as unit and method for the use thereof |
| US5287920A (en) * | 1992-06-16 | 1994-02-22 | Terrell Donna K | Large head downhole chemical cutting tool |
| US5320174A (en) * | 1992-06-16 | 1994-06-14 | Terrell Donna K | Downhole chemical cutting tool and process |
| US5444102A (en) * | 1993-03-05 | 1995-08-22 | Ikon Corporation | Fluoroiodocarbon blends as CFC and halon replacements |
| US5491028A (en) * | 1993-05-21 | 1996-02-13 | Trustees Of Boston University | Enhanced adherence of diamond coatings |
| US5520826A (en) * | 1994-05-16 | 1996-05-28 | The United States Of America As Represented By The Secretary Of The Navy | Flame extinguishing pyrotechnic and explosive composition |
| US5562764A (en) * | 1994-06-28 | 1996-10-08 | E. I. Du Pont De Nemours And Company | Process for preparing improved TIO2 by silicon halide addition |
| US5573744A (en) * | 1993-11-23 | 1996-11-12 | Kerr-Mcgee Corporation | Method for enhancing production of titanium dioxide |
| US20060273223A1 (en) * | 2005-01-12 | 2006-12-07 | Haaland Peter D | Fire suppression systems |
| USRE40651E1 (en) * | 1995-04-17 | 2009-03-10 | Eclipse Aviation Corporation | Labile bromine fire suppressants |
-
1995
- 1995-04-17 US US08/423,209 patent/US5626786A/en not_active Ceased
-
2004
- 2004-07-16 US US10/893,705 patent/USRE40651E1/en not_active Expired - Lifetime
-
2008
- 2008-10-31 US US12/263,122 patent/USRE41558E1/en not_active Expired - Lifetime
- 2008-10-31 US US12/263,054 patent/USRE41557E1/en not_active Expired - Lifetime
Patent Citations (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2732410A (en) * | 1956-01-24 | Process for preparing tetrafluoro | ||
| US955316A (en) * | 1907-07-26 | 1910-04-19 | Minimax Cons Ltd | Process of extinguishing burning benzin, &c. |
| US2791490A (en) * | 1952-04-29 | 1957-05-07 | Du Pont | Method and means for commingling and reacting fluid substances |
| US2918125A (en) * | 1955-05-09 | 1959-12-22 | William G Sweetman | Chemical cutting method and apparatus |
| US3076507A (en) * | 1958-05-16 | 1963-02-05 | William G Sweetman | Chemical cutting method and apparatus for use in wells |
| US3372208A (en) * | 1964-03-20 | 1968-03-05 | Dow Chemical Co | Flame resistant epoxy resins containing phosphorus and a halogen |
| US3266674A (en) * | 1964-08-24 | 1966-08-16 | Richard L Smith | Thermo-shave dispensing and reusable unit |
| US3479286A (en) * | 1965-09-22 | 1969-11-18 | Montedison Spa | Flame-extinguishing compositions |
| US3812239A (en) * | 1969-09-25 | 1974-05-21 | Ppg Industries Inc | Preparation of submicron titanium carbide |
| US3663283A (en) * | 1969-10-02 | 1972-05-16 | Richard A Hebert | Process and apparatus for the production of finely-divided metal oxides |
| US3637022A (en) * | 1969-10-30 | 1972-01-25 | Marathon Oil Co | Use of high water content oil-external micellar solutions for extinguishing fires |
| US3657030A (en) * | 1970-07-31 | 1972-04-18 | Bell Telephone Labor Inc | Technique for masking silicon nitride during phosphoric acid etching |
| US3903037A (en) * | 1972-08-31 | 1975-09-02 | Monsanto Co | Low melt viscosity self-extinguishing polymeric polyblend |
| US3985689A (en) * | 1973-05-25 | 1976-10-12 | Minnesota Mining And Manufacturing Company | Sorbent foam material |
| US4043950A (en) * | 1973-08-27 | 1977-08-23 | Wilmsen Hans | Process for the manufacture of plastic foams and flame-proofing foams characterized by the use of a carrier foam |
| US4129513A (en) * | 1974-07-09 | 1978-12-12 | The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Electric field responsive fluids |
| US3959741A (en) * | 1975-06-09 | 1976-05-25 | United Technologies Corporation | Interhalogen based combustion-driven laser which provides continuous wave output lasing from dual species |
| US4022872A (en) * | 1975-11-12 | 1977-05-10 | Ppg Industries, Inc. | Process for preparing finely-divided refractory powders |
| US4048290A (en) * | 1976-01-28 | 1977-09-13 | Cabot Corporation | Process for the production of finely-divided metal and metalloid oxides |
| US4250960A (en) * | 1977-04-18 | 1981-02-17 | Weatherford/Dmc, Inc. | Chemical cutting apparatus |
| US4125161A (en) * | 1977-04-18 | 1978-11-14 | Weatherford/Dmc, Inc. | Chemical cutting apparatus and method for use in wells |
| US4241042A (en) * | 1978-06-19 | 1980-12-23 | Montedison S.P.A. | Spherical titanium dioxide particles and process of manufacture |
| JPS569230A (en) * | 1979-06-28 | 1981-01-30 | Nippon Telegr & Teleph Corp <Ntt> | Manufacture of high purity quartz glass pipe |
| US4397977A (en) * | 1979-08-23 | 1983-08-09 | Pennwalt Corporation | Tetrahalophthalates as flame retardant plasticizers for halogenated resins |
| US4292290A (en) * | 1980-04-16 | 1981-09-29 | Cabot Corporation | Process for the production of finely-divided metal and metalloid oxides |
| US4428430A (en) * | 1981-01-13 | 1984-01-31 | Gearhart Industries, Inc. | Chemical method and apparatus for perforating drill collars |
| SU981338A1 (en) * | 1981-06-29 | 1982-12-15 | Всесоюзный научно-исследовательский институт противопожарной обороны МВД СССР | Combustion inhibitor |
| US4415029A (en) * | 1981-07-23 | 1983-11-15 | Gearhart Industries, Inc. | Downhole well tool and anchoring assembly |
| US4494601A (en) * | 1981-09-14 | 1985-01-22 | Gearhart Industries, Inc. | Downhole chemical cutting tool |
| US4406797A (en) * | 1981-11-03 | 1983-09-27 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Fire extinguishant materials |
| US4481119A (en) * | 1983-03-11 | 1984-11-06 | The United States Of America As Represented By The Secretary Of The Navy | Compositions for extinguishing titanium fires |
| US4619318A (en) * | 1984-09-27 | 1986-10-28 | Gearhart Industries, Inc. | Chemical cutting method and apparatus |
| US4822513A (en) * | 1984-11-12 | 1989-04-18 | Diversey Corporation | Cleaning/disinfecting process and composition |
| US5120689A (en) * | 1986-03-27 | 1992-06-09 | Imperial Chemical Industries Plc | Coked product containing domains of oxides |
| US5017525A (en) * | 1987-03-25 | 1991-05-21 | Imperial Chemical Industries Plc | Production of ceramic materials and of precursor therefor |
| US4819728A (en) * | 1987-09-01 | 1989-04-11 | Lafitte Louis D | Pressure relief system for down hole chemical cutters |
| US4949789A (en) * | 1987-09-01 | 1990-08-21 | Leon A. Robichaux | Pressure relief system for down hole chemical cutters |
| US5082575A (en) * | 1987-09-29 | 1992-01-21 | Shin-Etsu Handotai Company, Ltd. | Method for fire-extinguishment on hardly extinguishable burning materials |
| US4889187A (en) * | 1988-04-25 | 1989-12-26 | Jamie Bryant Terrell | Multi-run chemical cutter and method |
| US4971146A (en) * | 1988-11-23 | 1990-11-20 | Terrell Jamie B | Downhole chemical cutting tool |
| US5165916A (en) * | 1989-10-02 | 1992-11-24 | Phillips Petroleum Company | Method for producing carbide products |
| US5084190A (en) * | 1989-11-14 | 1992-01-28 | E. I. Du Pont De Nemours And Company | Fire extinguishing composition and process |
| US5219474A (en) * | 1989-11-17 | 1993-06-15 | Korea Institute Of Science And Technology | Liquid fire extinguishing composition |
| US5093013A (en) * | 1989-12-11 | 1992-03-03 | Halocarbon Products Corporation | Ozone friendly fire-extinguishing agents |
| US5192714A (en) * | 1990-02-14 | 1993-03-09 | Kabushiki Kaisha Toshiba | Method of manufacturing a multilayered metallization structure in which the conductive layer and insulating layer are selectively deposited |
| US5080177A (en) * | 1990-07-26 | 1992-01-14 | Great Lakes Chemical Corporation | Fire extinguishing methods utilizing 1-bromo-1,1,2,2-tetra-fluoroethane |
| US5135054A (en) * | 1990-10-05 | 1992-08-04 | University Of New Mexico | Fire extinguishing agents for flooding applications |
| US5235000A (en) * | 1990-12-10 | 1993-08-10 | Ethyl Corporation | Preparation, storage, and usage of bromine chloride |
| US5055208A (en) * | 1991-01-02 | 1991-10-08 | Powsus, Inc. | Fire extinguishing compositions |
| US5236611A (en) * | 1991-10-28 | 1993-08-17 | E. I. Du Pont De Nemours And Company | Mixtures of perfluoropropane and trifluoroethane |
| WO1993015794A1 (en) * | 1992-02-05 | 1993-08-19 | Ab Bejaro-Product | Gas-liquid mixture as well as unit and method for the use thereof |
| US5287920A (en) * | 1992-06-16 | 1994-02-22 | Terrell Donna K | Large head downhole chemical cutting tool |
| US5320174A (en) * | 1992-06-16 | 1994-06-14 | Terrell Donna K | Downhole chemical cutting tool and process |
| US5444102A (en) * | 1993-03-05 | 1995-08-22 | Ikon Corporation | Fluoroiodocarbon blends as CFC and halon replacements |
| US5491028A (en) * | 1993-05-21 | 1996-02-13 | Trustees Of Boston University | Enhanced adherence of diamond coatings |
| US5573744A (en) * | 1993-11-23 | 1996-11-12 | Kerr-Mcgee Corporation | Method for enhancing production of titanium dioxide |
| US5520826A (en) * | 1994-05-16 | 1996-05-28 | The United States Of America As Represented By The Secretary Of The Navy | Flame extinguishing pyrotechnic and explosive composition |
| US5562764A (en) * | 1994-06-28 | 1996-10-08 | E. I. Du Pont De Nemours And Company | Process for preparing improved TIO2 by silicon halide addition |
| USRE40651E1 (en) * | 1995-04-17 | 2009-03-10 | Eclipse Aviation Corporation | Labile bromine fire suppressants |
| US20060273223A1 (en) * | 2005-01-12 | 2006-12-07 | Haaland Peter D | Fire suppression systems |
| US20070119602A1 (en) * | 2005-01-12 | 2007-05-31 | Eclipse Aviation Corp. | Fire suppression systems |
| US20070119603A1 (en) * | 2005-01-12 | 2007-05-31 | Eclipse Aviation Corp. | Fire suppression systems |
| US20080115950A1 (en) * | 2005-01-12 | 2008-05-22 | Eclipse Aviation Corporation | Fire suppression systems |
Non-Patent Citations (14)
| Title |
|---|
| A.N. Baratov, A Review of Investigations on the Chemical Inhibition of Flames, Problems in Combustion and Extinguishment, 1968, 29-51, TsNIIPO MOOP, Moscow. * |
| Chemical Abstracts No. 117:134014, "Preparation of a Fire Extinguishing Composition", Valukonis et al. (1991). * |
| Chemical Abstracts No. 98:129086. "Combustion inhibitor for hydrocarbon-air Mixture", Petrova et al. (1982). * |
| CRC Handbook of Chemistry and Physics, 63rd Edition. pp. B-84, B-97, B-106, B-125, B-127, B-143, B-157, B-159 and C-525, (1982). * |
| D.R. Miller, et al., Effects of Various Inhibitors on Hydrogen-Air Flame Speeds, Combustion and Flame, Mar. 1963, 137-142, vol. 7, Butterworths, London. * |
| Final Technical Report FR-4021 Halogen Replacement for Aviation Systems, Peter D. Haaland & John H Huntington, May 1994-Nov. 1994. * |
| G. Lask & H. GG. Wagner, Influence of Additives on the Velocity of Laminar Flames, 8th Symposium (International) on Combustion, 1962, 432-438, Williams & Wilkens Co.,Baltimore. * |
| Hawley's Condensed Chemical Dictionary, 11u~ Edition, pp. 164, 169, 170, 173,329,642,913, and 1040, Van Nostrand Reinhold Company, N.Y. (1987). * |
| Hawley's Condensed Chemical Dictionary, 11u˜ Edition, pp. 164, 169, 170, 173,329,642,913, and 1040, Van Nostrand Reinhold Company, N.Y. (1987). * |
| Letter dated Aug. 15, 2006, from T. Howard to J. Sawtelle. * |
| Letter dated Aug. 18, 2006, from J. Sawtelle to T. Howard. * |
| The Montreal Protocol on Substances that Deplete the Ozone Layer, 2000, 1-47, UNEP Ozone Secretariat UN Environment Programme, Kenya. * |
| W.A. Rosser, et al., The Effect of Metal Salts on Premixed Hydrocarbon-Air Flames, Combustion and Flame, Mar. 1963, 107-119, vol. 7, Butterworths, London. * |
| W.A. Rosser, et al., The Quenching of Premixed Flames by Volatile Inhibitors, ICombustion and Flame, Mar. 1966, 287-294, vol. 10, Butterworths, London. * |
Also Published As
| Publication number | Publication date |
|---|---|
| US5626786A (en) | 1997-05-06 |
| USRE41558E1 (en) | 2010-08-24 |
| USRE40651E1 (en) | 2009-03-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| USRE41557E1 (en) | Labile bromine fire suppressants | |
| AU751975B2 (en) | Chemically active fire suppression composition | |
| US5465795A (en) | Fire suppressing apparatus for generating steam from a water-ice mixture | |
| US6217788B1 (en) | Fire suppression composition and device | |
| AU2005305380B2 (en) | Improved flame suppressant aerosol generant | |
| KR101562715B1 (en) | New method for extinguishing fire | |
| JPH06509492A (en) | Gas-liquid mixture, equipment and method for using it | |
| Zhang et al. | Hot aerosol fire extinguishing agents and the associated technologies: a review | |
| US3656553A (en) | Flame-extinguishing substance comprising 1,2-dibromohexafluropropane | |
| US8257607B1 (en) | Fluorocarbon-free, environmentally friendly, natural product-based, and safe fire extinguishing agent | |
| US3484372A (en) | Fire-extinguishing compositions | |
| EP0932432B1 (en) | Labile bromine fire suppressants | |
| JPH02265575A (en) | Extinguishing composition | |
| WO1993009848A1 (en) | Method for extinguishing fire with a breathable gas and water spray mixture | |
| CA2501457C (en) | Apparatus and method for suppressing a fire | |
| US5464544A (en) | Methods of extinguishing alkali metal fires with non-aqueous compositions | |
| CN114768163A (en) | Aerosol fire extinguishing agent | |
| Korostelev | Aerosol-generating pyrotechnic compositions with components interacting in the combustion wave | |
| Poynter | Halon replacements: Chemistry and applications | |
| Van Dolah et al. | Application of Halon 1301 to the Prevention of or Extinguishment of Aerozine-50 Fires | |
| JPS5829472A (en) | Powdery fire fighting agent |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: ECLIPSE AEROSPACE, INC., SOUTH CAROLINA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ECLIPSE AVIATION CORPORATION;REEL/FRAME:023220/0472 Effective date: 20090904 |
|
| AS | Assignment |
Owner name: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., G Free format text: SECURITY AGREEMENT;ASSIGNOR:ECLIPSE AEROSPACE, INC.;REEL/FRAME:023364/0639 Effective date: 20090902 Owner name: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A. AS Free format text: SECURITY AGREEMENT;ASSIGNOR:ECLIPSE AEROSPACE, INC.;REEL/FRAME:023364/0720 Effective date: 20090902 |
|
| AS | Assignment |
Owner name: WELLS FARGO BANK, NATIONAL ASSOCIATION, NORTH CARO Free format text: SECURITY INTEREST;ASSIGNOR:ECLIPSE AEROSPACE, INC.;REEL/FRAME:028641/0549 Effective date: 20120720 |
|
| AS | Assignment |
Owner name: WILMINGTON TRUST, NATIONAL ASSOCIATION, MINNESOTA Free format text: SECURITY INTEREST;ASSIGNOR:ECLIPSE AEROSPACE, INC.;REEL/FRAME:035450/0910 Effective date: 20150420 Owner name: WILMINGTON TRUST, NATIONAL ASSOCIATION, MINNESOTA Free format text: ASSIGNMENT OF PATENT AND TRADEMARK SECURITY AGREEMENT;ASSIGNOR:WELLS FARGO BANK, NATIONAL ASSOCIATION;REEL/FRAME:035470/0074 Effective date: 20150420 |
|
| AS | Assignment |
Owner name: CRYSTAL FINANCIAL SBIC LP, MASSACHUSETTS Free format text: ASSIGNMENT OF PATENT AND TRADEMARK SECURITY AGREEMENT;ASSIGNOR:WILMINGTON TRUST, NATIONAL ASSOCIATION;REEL/FRAME:036106/0876 Effective date: 20150708 |
|
| AS | Assignment |
Owner name: CANTOR FITZGERALD SECURITIES, FLORIDA Free format text: SECURITY INTEREST;ASSIGNOR:ECLIPSE AEROSPACE, INC.;REEL/FRAME:044177/0821 Effective date: 20171113 |
|
| AS | Assignment |
Owner name: CANTOR FITZGERALD SECURITIES, FLORIDA Free format text: ASSIGNMENT OF PATENT AND TRADEMARK SECURITY AGREEMENT;ASSIGNORS:ECLIPSE AEROSPACE, INC.;CRYSTAL FINANCIAL SBIC LP;REEL/FRAME:044512/0618 Effective date: 20171113 |