AU2103995A - Ozone friendly fire extinguishing methods and compositions - Google Patents
Ozone friendly fire extinguishing methods and compositionsInfo
- Publication number
- AU2103995A AU2103995A AU21039/95A AU2103995A AU2103995A AU 2103995 A AU2103995 A AU 2103995A AU 21039/95 A AU21039/95 A AU 21039/95A AU 2103995 A AU2103995 A AU 2103995A AU 2103995 A AU2103995 A AU 2103995A
- Authority
- AU
- Australia
- Prior art keywords
- fire
- composition
- extinguishing
- compositions
- fire extinguishing
- 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.)
- Abandoned
Links
Classifications
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62C—FIRE-FIGHTING
- A62C99/00—Subject matter not provided for in other groups of this subclass
- A62C99/0009—Methods of extinguishing or preventing the spread of fire by cooling down or suffocating the flames
- A62C99/0018—Methods of extinguishing or preventing the spread of fire by cooling down or suffocating the flames using gases or vapours that do not support combustion, e.g. steam, carbon dioxide
-
- 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
- A62D1/0057—Polyhaloalkanes
Landscapes
- Business, Economics & Management (AREA)
- Emergency Management (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Fire-Extinguishing Compositions (AREA)
Description
OZONE FRIENDLY FIRE EXTINGUISHING METHODS AND COMPOSITIONS
BACKGROUND OF THE INVENTION
FIELD OF THE INVENTION
The present invention relates to the field of fire extinguishing compositions and methods, and particularly to compositions and methods employing compositions comprised of hydrofluorocarbons and acid scavenging additives.
DESCRIPTION OF THE PRIOR ART
The use of certain bromine-containing chemical agents for the extinguishment of fires is common. These agents are in general thouglit to be effective due to their interference with the normal chain reactions responsible for flame propagation. The most widely accepted mechanism for flame suppression is the radical trap mechanism proposed by Fryburg in Review of
Literature Pertinent to Fire Extinguishing Agents and to Basic Mechanisms Involved in Their Action. NACA-TN 2102 (1950). lb is generally accepted that compounds containing bromine act by interfering with free radical or ionic species in the flame; the presence of fluorine has not been considered as contributing to the fire extinguishing properties of a compound, but will impart stability, reduce toxicity and boiling point, and increase thermal stability.
Various halogenated hydrocarbons have been employed as fire extinguishants . Prior to 1945, three halogenated
extinguishing agents widely used were carbon tetrachloride, methyl bromide and bro ochloromethane. For toxicological reasons, however, the use of these agents has been discontinued. The three fire extinguishing agents presently in common use are bromine-containing compounds, Halon 1301 (CF-Br), Halon 1211 (CF2BrCl) and Halon 2402 (BrCF„CF_Br) . The effectiveness of these three volatile bromine-containing compounds in extinguishing fires has been described in United States Patent No. 4,014,799, issued to Owens. The National Fire Protection Association (NFPA) publication, the Fire Protection Handbook, Section 18, Chapter 2, entitled "Halogenated Agents and Systems" (1985) describes these agents in more detail.
Although the above named bromine-containing compounds are effective fire fighting agents, those agents containing bromine or chlorine are asserted to be capable of the destruction of the earth's protective ozone layer. For example, Halon 1301 has an Ozone Depletion Potential (ODP) rating of 10, and Halon 1211 has an ODP of 3. As a result of concerns over ozone depletion, the production and sale of these agents after January 1, 1994 is prohibited under international and United States policy.
The use of hydrofluorocarbons as extinguishing agents has been proposed only recently, for example as described in U.S. Patent 5,124,053 to Iikubo and Robin. Since the hydro luorocarbons do not contain bromine or chlorine, the compounds have no effect on the stratospheric ozone layer and their ODP is zero. It has been discovered that certain of these compounds, especially those with a higher ratio of hydrogen to fluorine in the molecule, can decompose to some extent in a fire, producing hydrogen fluoride, HF, which is potentially damaging to personnel and equipment if formed in large quantities.
It is therefore an object of this invention to provide a method for extinguishing fires as rapidly and effectively as
the techniques employing presently employed fire extinguishing agents while avoiding the above-named drawbacks
It is a further object of this invention to provide an agent for use in a method of the character described that is efficient, economical and environmentally safe with regard to ozone depletion.
SUMMARY OF THE INVENTION
Briefly describing one aspect of the present invention there is provided a method of extinguishing a fire that comprises introducing to the fire a fire extinguishing concentration of an extinguishant composition comprising, and preferably consisting essentially of, a hydrofluorocarbon and an acid-scavenging additive, and maintaining the concentration of the composition until the fire is extinguished. Fire extinguishing compositions comprising, or consisting essentially of, a hydrofluorocarbon and an acid-scavenging additive are also provided.
It is an object of the present invention to provide an effective method for extinguishing fires. Another object of the present invention is to provide a fire extinguishing method which utilizes particular combinations of hydro luorocarbons and acid-scavenging additives which are effective at non-toxic levels.
It is a further object of the present invention to provide a fire extinguishing method which employs compounds that are environmentally safe, having low ozone depletion potential and greenhouse warming effect.
A further object of the present invention is to provide fire extinguishing compositions comprising blends of hydrofluorocarbons and acid-scavenging additives, which blends are effective and safe in use.
A further object of the present invention is to provide fire extinguishing compositions which produce reduced amounts of decomposition products compared to other fire extinguishing agents when employed in the extinguishment of fires.
Further objects of the present invention will be apparent from the description which follows.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
For the purpose of promoting an understanding of the principles of the invention, reference will now be made to preferred embodiments of the invention and specific language will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended, such alterations, further modi ications and applications of the principles of the invention as described herein being contemplated as would normally occur to one skilled in the art to which the invention relates. In accordance with the present invention, it has been found that compositions comprising a hydrofluorocarbon in combination with an acid-scavenging additive provide particularly effective fire extingiiishants at concentrations safe for use. Because the compositions contain no bromine or chlorine, they have an ozone depletion potential of zero. In addition, the compositions produce less decomposition products than the hydrofluorocarbon analogs, and hence are of reduced toxicity with regard to use in a fire scenario. In a related aspect, the invention relates to methods for extinguishing fires which are improved by using these compositions as the fire extinguishing agents.
The invention is directed to a non-toxic fire extinguishant comprising in combination: (a) a hydrofluorocarbon of the formula CxHyFz , wherein (y+z) = (2x + 2), and wherein y x; and
(b) one or more substances selected from the group consisting of terpenes, unsaturated oils, sodium bicarbonate, potassium bicarbonate, monoammonium phosphate, alkali metal halides and urea. The extinguishant compositions may preferably consist essentially of the hydro luorocarbon and the acid-scavenger(s) .
Specific hydrofluorocarbons useful in accordance with the present invention include trifluoromethane (CF-H), pentafluoroethane (CF CF II) , 1, 1, 1,2-tetrafluoroethane (CF3CH2F) , 1,1, 1,2,3,3-hexafluoropropane (CF3CHFCF2H) , 1, 1,1,3,3,3-hexafluoropropane (CF CH CF ) , 1, 1,2,2,3,3-hexafluoropropane (HCF2CF2CF2H) , 1,1, 1,2, 3,3, 3-heptafluoropropane (CF3CHFCF_) , 1,1, 1, 2,2,3,3-heptafluoropropane (CF CF.CF H) , 1,1, 1,2,2,3,3,4,4-nonafluorobutane (CF3CF2CF2CF2II) , 1, 1,1,2,3,4,4, -octafluorobutane (CF3CHFCHFCF3) and 1, 1,1,3,3, 3-hexafluorobutane ( F_CH2CH2CF3) . Other hydrofluorocarbons within the present invention are C3H3F5, C4I.3F7. 5HF3Fπ, C^F^, C5H3F9, C5H4FB. and C^I^. Specific terpenes useful in accordance with the present invention include citral, citronellal, limonene, dipentene, menthol, alpha-pinene, beta-pinene, camphor, vitamin A beta-carotene, and isoproρenyl-1-methylcyclohexene. The terpenes preferably comprise from about 0.1% to about 10% by weight of the extinguishing composition.
Specific unsaturated oils useful in accordance witli the present invention include oleic acid, linoleic acid, palinitoleic acid and vaccenic acid. The unsaturated oils preferably comprise from about 0.1% to about 10% by weight of the extinguishing composition.
Specific alkali metal halides useful in accordance with the present invention include sodium chloride, potassium chloride, sodium bromide and potassium bromide. The alkali metal halides preferably comprise from about 0.1% to about 10% by weight of the extinguishing composition.
In accordance with one embodiment of the present invention, there is provided a method for extinguishing fires which includes the use of a composition comprised of a hydrofluorocarbon and an acid-scavenging additive as a fire
ext nguishing agent. The compositions may be applied in the variety of methods employed for other halogenated hydrocarbons, including application in a flooding system, portable system or specialized system. The extinguishant is effective in low concentrations, and of course, at high concentrations as well. The concentration employed may depend to some extent on the nature of the fire, the combusting material and tiie circumstances of application. Generally, application rates preferably range from about 1% to about 25% v/v, and more preferably from about 2% and to about 15% v/v, of the hydrofluorocarbon component in the atmosphere. The acid-scavenging additives comprise from about 0.1% to about 10% by weight of the composition.
The relative amounts of the hydrofluorocarbon and the acid-scavenging additive are not critical, but rather are dictated by the characteristics desired for the overall composition. For example, in certain applications there may be a greater need for low toxicity, and in other instances, the emphasis may be on cleanliness of the extinguishment . The methods for application of the described fire extinguishing compositions are those known to be useful for the Halon agents. In broad terms, these methods utilize application systems which typically include a supply of agent, a means for releasing or propelling the agent from its container, and one or more discharge nozzles to apply the agent into the hazard or directly onto the burning object. Thus, the agents of this invention may be used in total flooding systems in which the agent is introduced into an enclosed region surrounding a fire at a concentration sufficient to extinguish the fire. In accordance with a total flooding system, equipment or even rooms may be provided with a source of agent and appropriate piping, valves and controls so as to automatically and/or manually be introduced at appropriate concentrations in the event that fire should break out. As is known to those skilled in the
art, the fire extinguishant may be pressurized with nitrogen or other inert gas at up to about 600 psig at ambient conditions.
Alternatively, the compositions of the invention may be applied to a fire through the use of conventional portable fire extinguishing equipment. It is usual to increase the pressure in portable fire extinguishers with nitrogen or other inert gases in order to ensure that the agent is completely expelled from the extinguisher. Systems in accordance witli this invention may be conveniently pressurized at any desirable pressure up to about 600 psig at ambient conditions.
The invention will be further described with reference to the following specific Examples. However, it will be understood that these Examples are illustrative and not restrictive in nature.
EXAMPLE 1 A test facility with a total internal volume of 1440 cubic feet was constructed from 2x4 lumber and 3/4" plywood. The enclosure was equipped with two 3 foot by 3 foot windows and two standard doors located on opposite walls. The delivery system consisted of a standard Halon cylinder connected to 1" carbon steel pipe via a stainless steel flexhose, terminating in a standard Halon nozzle located 6 inches down from the center of the ceiling.
A large steel pan was filled with commercial n-heptane and placed in the center of the facility, and the n-heptane was then ignited. Thirty seconds after ignition, the doors to the enclosure were closed and the extinguishing agent released. The enclosure atmosphere was sampled after extinguishment of the fire by pulling a sample of the post-extinguishment atmosphere through a buffer solution contained in a polypropylene bubbler equipped with a 70 micron porous polyethylene frit. Fluoride and HF concentrations were determined employing a fluoride ion
selective electrode (ISE). The post-extinguishment atmosphere was sampled at two locations, one at a height of 6 feet and the second at a height of 2 feet, both sampling points located 2 feet diagonally out from the corner of the enclosure.
Sixty nine pounds of 1, 1, 1,2, 3, 3, 3-heptafluoropropane (CF3CHFCF_) was discharged according to the above procedure and resulted in extinguishment of the fire. Analysis showed the concentration of HF to be 3535 ppm at the 6 foot location and 1948 ppm at the 2 foot location.
EXAMPLE 2 The procedure of Example 1 was repeated employing G9 pounds of 1, 1, 1,2, 3,3 ,3-heptafluoropropane (CF CHFCF ) to which had been added 1.0 pounds of dipeutene (1.4 % by weight) . Analysis showed the concentration of HF to be 2403 ppm at the 6 foot location and 1202 ppm at the 2 foot location.
This example demonstrates the advantageous effect of the addition of a small amount of an acid-scavenging additive to the hydrofluorocarbon. The amount of HF produced was reduced by 32% at the 6 foot location and by 38% at the 2 foot location.
EXAMPLE 3 The procedure of Example 1 was repeated employing a small steel pan filled with n-heptane. Analysis of the post-extinguishment atmosphere showed a concentration of HF of 50 ppm at the 6 foot location and 11 ppm at the 2 foot location.
EXAMPLE 4 The procedure of Example 3 was repeated employing 69 pounds of 1, 1,1,2,3,3,3-heptafluoropropane (CF-CHFCF..,) to which had been added 1.0 pounds of limonene (1.4 % by
weight) . Following extinguishment of the fire, analysis showed the concentration of HF to be 32 ppm at the 6 foot location and 7 ppm at the 2 foot location.
This example demonstrates the advantageous effect of the addition of a small amount of an acid-scavenging additive to the hydrofluorocarbon. The amount of HF produced was reduced by 36% at botli locations.
EXAMPLE 5 Testing of the fire suppressing and extinguishing capabilities of 1, 1, 1,2,3,3, 3-heptafluoropropane with each of the following acid-scavengers yields similarly advantageous results: citral, citronellal, menthol, alpha-p nene, beta-pinene, camphor, vitamin A beta-carotene, isopoopenyl-1-l-methylcyclohexene, oleic acid, linoleic acid, palmitoleic acid, vaccenic acid, sodium chloride, potassium chloride, sodium bromide and potassium bromide. Desirable results are achieved for combinations of 90% to 99.9% by weight of the 1, 1, 1 , 2,3,3 , 3-heptafluoropropane and of 0.1% to 10.0% of the acid-scavenger. Similarly, suitable results are obtained for fire extinguishant compositions comprising blends of the foregoing ac d-scavengers and the various other hydrofluorocarbons defined herein, including for example, trifluoromethane, pentafluoroethane, 1,1,1, 2-tetrafluoroethane, 1,1,1,2,3,3-hexafluoropropane, 1,1,1,3,3,3-hexafluoropropane, 1,1,2,2,3, 3-hexafluoropropane, 1,1,1,2,2,3 ,3-heptafluoropropane, 1,1,1,2,2,3,3,4,4-nonafluorobutane, 1,1,1,2,3,4,4,4-octafluorobutane and 1, 1, 1,3,3, 3-hexafluorobutane. The foregoing compositions are effective in both total flooding and portable fire extinguishing systems, and work conventionally with typical, known propellants.
Claims (8)
1. A method for extinguishing a fire comprising the steps of: a. introducing to the fire a fire extinguishing concentration of a composition comprising in combination:
(i) one or more hydrofluorocarbons of the formula
C II F , wherein (y+z) = (2x + 2), and wherein y _ x; _x y z and
(ii) one or more substances selected from the group consisting of terpenes, unsaturated oils, sodium bicarbonate, potassium bicarbonate, monoammonium phosphate, alkali metal halides and urea; and b. maintaining the concentration of the composition until the fire is extinguished.
2. The process of claim 1 wherein the composition is employed at a level of less than about 25% v/v of the hydro luorocarbons.
3. The process of claim 1 wherein the extinguishing concentration of the compound is from about 1% to about 15% v/v of the hydrofluorocarbons.
4. The process of claim 1 wherein the composition is introduced by a total flooding system.
5. The process of claim 1 wherein the composition is introduced by a portable extinguishing system.
6. The process of claim 1 wherein the composition contains from about 90 to 99.9 percent by weight hydrofluorocarbon.
7. The process of claim 1 wherein the composition contains from about 0.1 to about 10 percent by weight of one or more of the substances selected from the group consisting of terpenes, unsaturated oils, sodium bicarbonate, potassium bicarbonate, monoammonium phosphate, alkali metal halides and urea.
8. The process of claim 1 wherein the composition consists essentially of from about 90% to about 99.9% by weight of said hydrofluorocarbon and from about 0.1% to about 10.0% of said substance.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21834794A | 1994-03-28 | 1994-03-28 | |
US218347 | 1994-03-28 | ||
PCT/US1995/003490 WO1995026218A1 (en) | 1994-03-28 | 1995-03-21 | Ozone friendly fire extinguishing methods and compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2103995A true AU2103995A (en) | 1995-10-17 |
Family
ID=22814744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU21039/95A Abandoned AU2103995A (en) | 1994-03-28 | 1995-03-21 | Ozone friendly fire extinguishing methods and compositions |
Country Status (13)
Country | Link |
---|---|
EP (1) | EP0752900A1 (en) |
JP (1) | JPH09510891A (en) |
KR (1) | KR970702089A (en) |
AU (1) | AU2103995A (en) |
CA (1) | CA2185910A1 (en) |
HU (1) | HU9602662D0 (en) |
IL (1) | IL113086A0 (en) |
MX (1) | MX9604320A (en) |
NO (1) | NO964046L (en) |
NZ (1) | NZ283089A (en) |
PL (1) | PL316629A1 (en) |
WO (1) | WO1995026218A1 (en) |
ZA (1) | ZA952385B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1283203B1 (en) * | 1996-03-07 | 1998-04-16 | Ausimont Spa | FIRE EXTINGUISHING COMPOSITIONS |
IT1282378B1 (en) * | 1996-04-24 | 1998-03-20 | Ausimont Spa | DIOXIDE-BASED PERFLUOROELASTOMERS |
ITMI981505A1 (en) * | 1998-06-30 | 1999-12-30 | Ausimont Spa | PURIFICATION OF FLUORINATED POLYMERS |
ITMI981506A1 (en) | 1998-06-30 | 1999-12-30 | Ausimont Spa | AMORPHOUS FLUOROPOLYMER MANUFACTURES |
IT1312320B1 (en) | 1999-05-25 | 2002-04-15 | Ausimont Spa | (PER) FLUORINATED AMORPHOUS POLYMER MEMBRANES. |
US7405334B2 (en) | 2003-05-23 | 2008-07-29 | E. I. Du Pont De Nemours And Company | Process for the reduction of acidic contaminates in fluorinated hydrocarbons |
US20060016608A1 (en) * | 2004-07-21 | 2006-01-26 | Kidde Ip Holdings Limited | Discharge of fire extinguishing agent |
IT1391013B1 (en) * | 2008-07-01 | 2011-10-27 | Explosafe Int B V | EXTINGUISHING AGENTS BASED ON FLUOROIODO-CARBIDE BLENDS ADDITIVATED WITH DETOXIFYING COMPOUNDS. |
US9302128B2 (en) | 2011-10-25 | 2016-04-05 | Kidde Technologies, Inc. | Automatic fire extinguishing system with internal dip tube |
US9192798B2 (en) | 2011-10-25 | 2015-11-24 | Kidde Technologies, Inc. | Automatic fire extinguishing system with gaseous and dry powder fire suppression agents |
US9463341B2 (en) | 2011-10-25 | 2016-10-11 | Kidde Technologies, Inc. | N2/CO2 fire extinguishing system propellant gas mixture |
US9308406B2 (en) | 2011-10-25 | 2016-04-12 | Kidde Technologies, Inc. | Automatic fire extinguishing system having outlet dimensions sized relative to propellant gas pressure |
US9168406B2 (en) | 2012-03-15 | 2015-10-27 | Kidde Technologies, Inc. | Automatic actuation of a general purpose hand extinguisher |
WO2016195635A1 (en) * | 2015-05-29 | 2016-12-08 | Sevo Systems, Inc. | Method for delivering and extinguishing composition to a fire |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE789667A (en) * | 1971-10-08 | 1973-04-04 | Rhone Progil | LIQUID EXTINGUISHING COMPOSITION BASED ON HALOGENOUS HYDROCARBONS |
GB8600853D0 (en) * | 1986-01-15 | 1986-02-19 | Thacker D A | Fire extinguishant formulation |
US4954271A (en) * | 1988-10-06 | 1990-09-04 | Tag Investments, Inc. | Non-toxic fire extinguishant |
US5124053A (en) * | 1989-08-21 | 1992-06-23 | Great Lakes Chemical Corporation | Fire extinguishing methods and blends utilizing hydrofluorocarbons |
US5141654A (en) * | 1989-11-14 | 1992-08-25 | E. I. Du Pont De Nemours And Company | Fire extinguishing composition and process |
US5084190A (en) * | 1989-11-14 | 1992-01-28 | E. I. Du Pont De Nemours And Company | Fire extinguishing composition and process |
-
1995
- 1995-03-21 EP EP95913781A patent/EP0752900A1/en not_active Withdrawn
- 1995-03-21 NZ NZ283089A patent/NZ283089A/en unknown
- 1995-03-21 PL PL95316629A patent/PL316629A1/en unknown
- 1995-03-21 CA CA002185910A patent/CA2185910A1/en not_active Abandoned
- 1995-03-21 WO PCT/US1995/003490 patent/WO1995026218A1/en not_active Application Discontinuation
- 1995-03-21 MX MX9604320A patent/MX9604320A/en unknown
- 1995-03-21 JP JP7525205A patent/JPH09510891A/en active Pending
- 1995-03-21 AU AU21039/95A patent/AU2103995A/en not_active Abandoned
- 1995-03-21 HU HU9602662A patent/HU9602662D0/en unknown
- 1995-03-22 IL IL11308695A patent/IL113086A0/en unknown
- 1995-03-23 ZA ZA952385A patent/ZA952385B/en unknown
-
1996
- 1996-09-25 KR KR1019960705361A patent/KR970702089A/en not_active Application Discontinuation
- 1996-09-26 NO NO964046A patent/NO964046L/en unknown
Also Published As
Publication number | Publication date |
---|---|
CA2185910A1 (en) | 1995-10-05 |
PL316629A1 (en) | 1997-02-03 |
EP0752900A1 (en) | 1997-01-15 |
MX9604320A (en) | 1997-06-28 |
NO964046D0 (en) | 1996-09-26 |
NO964046L (en) | 1996-09-26 |
ZA952385B (en) | 1995-12-14 |
JPH09510891A (en) | 1997-11-04 |
IL113086A0 (en) | 1995-06-29 |
KR970702089A (en) | 1997-05-13 |
WO1995026218A1 (en) | 1995-10-05 |
HU9602662D0 (en) | 1996-11-28 |
NZ283089A (en) | 1997-07-27 |
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