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
  • A62D1/0057—Polyhaloalkanes

Definitions

• This invention relates to fire extinguishing methods and blends utilizing higher fluorinated C 2 and C 3 saturated hydrofluorocarbons.
• hydrofluorocarbons i.e., compounds containing only C, H and F atoms
• hydrofluorocarbons i.e., compounds containing only C, H and F atoms
• iodine-containing compounds as fire extinguishing agents has been avoided primarily due to the expense of their manufacture or due to toxicity considerations.
• the three fire extinguishing agents presently in common use are all bromine-containing compounds, Halon 1301 (CF 3 Br) , Halon 1211 (CF 2 BrCl) and Halon 2402 (CF 2 BrCF 2 Br) .
• the effectiveness of these three volatile bromine-containing compounds in extinguishing fires has been described in U.S. Patent 4,014,799 to Owens.
• certain chlorine-containing compounds are also known to be effective extinguishing agents, for example Halon 251 (CF 3 CF 2 C1) as described by Larsen in U.S. Patent 3,844,354.
• bromine-containing Halons are effective fire fighting agents, those agents containing bromine or chlorine are asserted by some to be capable of the destruction of the earth's protective ozone layer. Also, because the agents contain no hydrogen atoms which would permit their destruction in the troposphere, the agents may also contribute to the greenhouse warming effect. It is therefore an object of this invention to provide a method for extinguishing fires that extinguishes fires as rapidly and effectively as the techniques employing presently used Halon agents while avoiding the above-named drawbacks. It is a further object of this invention to provide an agent for the use in a method of the character described that is efficient, economical to manufacture, and environmentally safe with regard to ozone depletion and greenhouse warming effects. It is a still further object of this invention to provide blends of hydrofluorocarbons and other fire extinguishing agents that are effective and environmentally safe.
• the foregoing and other objects, advantages and features of the present invention may be achieved by employing saturated, higher fluorinated hydrofluorocarbons and blends thereof with other agents as fire extinguishants for use in fire extinguishing methods and apparatus. More particularly, the method of this invention involves introducing to a fire a saturated C 2 or C 3 higher fluorinated hydrofluorocarbon in a fire extinguishing concentration and maintaining such concentration until the fire is extinguished.
• Saturated higher fluorinated hydrofluorocarbons of this invention include compounds of the formula C ⁇ H y F z , where x is 2 or 3; y is 1 or 2; and z is 5, 6 or 7; where y is 1 and z is 5 when x is 2 and where z is 6 or 7 when x is 3.
• hydrofluorcarbons useful in accordance with this invention include heptafluoropropane (CF 3 CHFCF 3 ) , 1,1,1,3,3,3-hexafluoropropane (CF 3 CH 2 CF 3 ) , 1,1,1,2,3,3-hexafluoropropane (CF 3 CHFCHF 2 ) and pentafluoroethane (CF 3 CHF 2 ) .
• CF 3 CHFCF 3 1,1,1,3,3,3-hexafluoropropane
• CF 3 CHFCHF 2 1,1,1,2,3,3-hexafluoropropane
• pentafluoroethane CF 3 CHF 2
• saturated higher fluorinated C 2 and C 3 hydrofluorocarbons have been found to be effective fire extinguishants at concentrations safe for use.
• hydrofluorocarbons contain no bromine or chlorine, they have an ozone depletion potential of zero.
• the compounds contain hydrogen atoms, they are susceptible to breakdown in the lower atmosphere and hence do not pose a threat as greenhouse warming gasses.
• Specific hydrofluorocarbons useful in accordance with this invention are compounds of the formula C ⁇ H y F z , where x is 2 or 3; y is 1 or 2; and z is 5, 6 or 7; where y is 1 and z is 5 when x is 2; and where z is 6 or 7 when x is 3.
• Specific hydrofluorcarbons useful in accordance with this invention include heptafluoropropane (CF 3 CHFCF 3 ) , 1,1,1,3,3,3-hexafluoro ⁇ propane (CF 3 CH 2 CF 3 ), 1,1,1,2,3,3-hexafluoropropane (CF 3 CHFCHF 2 ) , and pentafluoroethane (CF 3 CHF 2 ) .
• hydrofluorocarbons of this invention may be used alone or in admixture with each other or in blends with other fire extinguishing agents.
• agents with which the hydrofluorocarbons of this invention may be blended are chlorine and/or bromine containing compounds such as Halon 1301 (CF 3 Br) , Halon 1211 (CF 2 BrCl) , Halon 2402
• hydrofluorocarbons of this invention are employed in blends, they are desirably present at a level of at least about 10 percent by weight of the blend.
• the hydrofluorocarbons are preferably employed at higher levels in such blends so as to minimize the adverse environmental effects of chlorine and bromine containing agents.
• hydrofluorocarbon compounds used in accordance with this invention are non-toxic and are economical to manufacture.
• the saturated highly fluorinated C 2 and C ⁇ hydrofluorocarbons of this invention may be effectively employed at substantially any minimum concentrations at which fire may be extinguished, the exact minimum level being dependent on the particular combustible material, the particular hydrofluorocarbon and the combustion conditions.
• hydrofluorocarbons or mixtures and blends thereof are employed at a level of at least about 3% (v/v) .
• hydrofluorocarbons alone best results are achieved with agent levels of at least about 5% (v/v) .
• the maximum amount to be employed will be governed by matters of economics and potential toxicity to living things.
• About 15% (v/v) provides a convenient maximum concentration for use of hydrofluorocarbons and mixtures and blends thereof in occupied areas. Concentrations above 15 % (v/v) may be employed in unoccupied areas, with the exact level being determined by the the particular combustible material, the hydrofluorocarbon (or mixture or blend thereof) chosen and the conditions of combustion.
• the preferred concentration of the hydrofluorocarbon agents, mixtures and blends in accordance with this invention lies in the range of about 5 to 10% (v/v) .
• Hydrofluorocarbons may be applied using conventional application techniques and methods used for Halons such as Halon 1301 and Halon 1211.
• these agents may be used in a total flooding fire extinguishing system in which the agent is introduced to an enclosed region (e.g., a room or other enclosure) surrounding a fire at a concentration sufficient to extinguish the fire.
• equipment or even rooms or enclosures may be provided with a source of agent and appropriate piping, valves, and controls so as automatically and/or manually to be introduced at appropriate concentrations in the event that fire should break out.
• the fire extinguishant may be pressurized with nitrogen or other inert gas at up to about 600 psig at ambient conditions.
• the hydrofluorocarbon agents 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 gasses in order to insure that the agent is completely expelled from the the extinguisher. Hydrofli -jrocarbon containing systems in accordance with this ii;mention may be conveniently pressurized at any desirable pressure up to about 600 psig at ambient conditions.
• EXAMPLE 1 A 28.3 cubic litre test enclosure was constructed for static flame extinguishment tests (total flooding) .
• the enclosure was equipped with a Plexiglas viewport and an inlet at the top for the agent to be tested and an inlet near the bottom to admit air.
• a 90 x 50 mm glass dish was placed in the center of the enclosure and filled with 10 grams of cigarette lighter fluid available under the trademark RONSONOL.
• the fuel was ignited and allowed a 15 second preburn before introduction of the agent. During the preburn, air was admitted to the enclosure through the lower inlet. After 15 seconds, the air inlet was closed and the fire extinguishing agent was admitted to the enclosure.
• a predetermined amount of agent was delivered sufficient to provide 6.6% v/v concentration of the agent.
• the extinguishment time was measured as the time between admitting the agent and extinguishment of the flame. Average extinguishment times for a 6.6% v/v concentration of heptafluoropropane, Halon 1301, Halon 1211 and CF 3 CHFBr are given in Table 1.
• Example 2 The experimental procedure of Example 1 was carried out employing heptane as the fuel. The average extinguishment times for 6.6% v/v of the s ⁇ une agents are also given in Table 1.
• the Table shows the extinguishment time required for various fuels at 6.6% v/v of the agents employed. At this level, heptafluoropropane is as effective as bromine-containing Halons in extinguishing an n-heptane flame and nearly effective as the other agents in extinguishing lighter fluid flames.
• Levels of about 5-10% are preferred for general application of pure hydrofluorocarbons in accordance with this invention.
• the use of too little agent results in failure to extinguish the fire and can result in excessive smoke and probably release of HF due to combustion of the agent.
• the use of excessive amounts is wasteful and can lead to dilution of the oxygen level of the air to levels harmful to living things.
• Example 1 was repeated with two white mice admitted to the chamber. After extinguishment, mice were exposed to combustion products for a total of 10 minutes before being removed from the chamber. All mice showed no ill effects during the exposure and appeared to behave normally after removal from the apparatus.
• Halon 1211 and Halon 251 were used to extinguish n-heptane diffusion flames using the method of Example 4. Test data are reported in Table 3.
• heptafluoropropane 1,1,1,2,3,3-hexafluoropropane and pentafluoroethane in accordance with this invention is significantly more effective than other known non-bromine or chlorine containing Halons such as Halon 14 (CF 4 ) .
• heptafluoropropane is comparable in effectiveness to Halon 251, a chlorine containing chlorofluorocarbon. The latter relationship is shown with respect to n-heptane as well as n-butane fuels.
• 1,1,1,3,3,3-hexafluoropropane is a highly effective fire extinguishant. It is nearly as effective as Halon 251, a chlorofluorocarbon, and it is sufficiently effective, when compared to bromine containing Halons such as Halon 1301 and Halon 1211, that it is preferable by reason of the absence of ozone depletion and other environmental effects of the chlorine and bromine containing Halons.
• 1.1.1.2.3.3-hexafluoropropane at concentrations in accordance with the method of this invention is well within the range of toxicological safety.
• the following Examples demonstrate the effective use of hydrofluorocarbon agents in accordance with this invention in mixtures or blends including bromine-containing Halon fire extinguishants.
• Table 6 reports the actual volume percent in air as observed. Table 6 also reports the calculated weight percent heptafluoropropane in the mixture. In addition. Table 6 also reports the ozone depletion potential ("ODP") for each agent.
• 1,1,1,3,3,3-hexafluoropropane and pentafluoroethane like the presently employed chlorine and bromine-containing Halons, are nondestructive agents, and are especially useful where cleanup of other media poses a problem.
• Some of the applications of the hydrofluorocarbons of this invention. are the extinguishing of liquid and gaseous fueled fires, the protection of electrical equipment, ordinary combustibles such as wood, paper and textiles, hazardous solids, and the protection of computer facilities, data processing equipment and control rooms.

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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Business, Economics & Management (AREA)
• Emergency Management (AREA)
• Fire-Extinguishing Compositions (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Fire-Extinguishing By Fire Departments, And Fire-Extinguishing Equipment And Control Thereof (AREA)
• Measuring Volume Flow (AREA)
• Catalysts (AREA)
• Fireproofing Substances (AREA)
• Ultra Sonic Daignosis Equipment (AREA)

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• 1990
  • 1990-08-09 EP EP90912103A patent/EP0439579B1/de not_active Revoked
  • 1990-08-09 AU AU61719/90A patent/AU629975B2/en not_active Expired
  • 1990-08-09 AT AT90912103T patent/ATE129419T1/de active
  • 1990-08-09 JP JP2511655A patent/JP2580075B2/ja not_active Expired - Lifetime
  • 1990-08-09 DK DK90912103.0T patent/DK0439579T3/da active
  • 1990-08-09 DE DE69023220T patent/DE69023220T2/de not_active Revoked
  • 1990-08-09 ES ES90912103T patent/ES2078348T3/es not_active Expired - Lifetime
  • 1990-08-09 BR BR909006888A patent/BR9006888A/pt not_active IP Right Cessation
  • 1990-08-09 WO PCT/US1990/004467 patent/WO1991002564A1/en not_active Application Discontinuation
  • 1990-08-09 RU SU4895510/63A patent/RU2293583C2/ru active IP Right Maintenance
  • 1990-08-14 IL IL95365A patent/IL95365A/xx active IP Right Grant
  • 1990-08-15 CA CA002023333A patent/CA2023333C/en not_active Expired - Lifetime
  • 1990-08-20 MX MX022023A patent/MX172050B/es unknown
• 1991
  • 1991-04-19 FI FI911915A patent/FI103182B1/fi active
  • 1991-04-22 NO NO911579A patent/NO177888C/no unknown
• 1998
  • 1998-08-18 KR KR1019980706409A patent/KR100189484B1/ko not_active IP Right Cessation

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