US3647001A - Combating fire with ablative water - Google Patents
Combating fire with ablative water Download PDFInfo
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- US3647001A US3647001A US30835A US3647001DA US3647001A US 3647001 A US3647001 A US 3647001A US 30835 A US30835 A US 30835A US 3647001D A US3647001D A US 3647001DA US 3647001 A US3647001 A US 3647001A
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract description 76
- 239000004094 surface-active agent Substances 0.000 claims abstract description 29
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 10
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 35
- 238000009736 wetting Methods 0.000 abstract description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 15
- 239000003349 gelling agent Substances 0.000 description 12
- 229940117927 ethylene oxide Drugs 0.000 description 8
- 229920006037 cross link polymer Polymers 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 239000007859 condensation product Substances 0.000 description 4
- 239000003599 detergent Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 230000035515 penetration Effects 0.000 description 4
- -1 poly(ethylene oxides) Polymers 0.000 description 4
- 230000009471 action Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- SIDULKZCBGMXJL-UHFFFAOYSA-N 1-dimethylphosphoryldodecane Chemical compound CCCCCCCCCCCCP(C)(C)=O SIDULKZCBGMXJL-UHFFFAOYSA-N 0.000 description 1
- CJPDBKNETSCHCH-UHFFFAOYSA-N 1-methylsulfinyldodecane Chemical compound CCCCCCCCCCCCS(C)=O CJPDBKNETSCHCH-UHFFFAOYSA-N 0.000 description 1
- XSXWOBXNYNULJG-UHFFFAOYSA-N 2-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC(C)(C)CC(C)(C)C1=CC=CC=C1O XSXWOBXNYNULJG-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910001508 alkali metal halide Inorganic materials 0.000 description 1
- 150000008045 alkali metal halides Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical class [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052622 kaolinite Inorganic materials 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000011176 pooling Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Images
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
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62C—FIRE-FIGHTING
- A62C3/00—Fire prevention, containment or extinguishing specially adapted for particular objects or places
- A62C3/06—Fire prevention, containment or extinguishing specially adapted for particular objects or places of highly inflammable material, e.g. light metals, petroleum products
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62C—FIRE-FIGHTING
- A62C35/00—Permanently-installed equipment
- A62C35/58—Pipe-line systems
- A62C35/60—Pipe-line systems wet, i.e. containing extinguishing material even when not in use
- A62C35/605—Pipe-line systems wet, i.e. containing extinguishing material even when not in use operating and sounding alarm automatically
Definitions
- An ablative material as comprehended within the present invention is a material which, when present in a layer of sufficient thickness, will permit thermal energy to be transmitted through its exposed outer surface but not completely through said layer, said thermal energy being absorbed within said layer so as to immediately transform the material of said layer into vapor without internal convection of said material, said vapor leaving said layer through its outer surface.
- ablative fluid material As described in the aforementioned Livingston et al. application water is converted to an ablative fluid material by the admixture therewith of a water-swellable cross-linked polymer.
- the formed ablative fluid material is in the form of a gel and is denoted ablative water.
- Water-swellable cross-linked polymers useful as gelling agents to convert water to ablative water are described in Katzer U.S. Pat. No. 3,354,084 and Bashaw et al. U.S. Pat. No. 3,229,769.
- One useful water-swellable cross-linked polymer is sold by B. F. Goodrich Chemical Company under the designation Carbopol-960.
- Another useful water-swellable cross-linked polymer is sold by Dow Chemical under the designation of Gelgard M. Gelgard M is described in my copending application Ser. No. 13,179 filed Feb. 20, 1970 titled Slurry Additive for Ablative Water Fire Extinguishing Systems.
- the ablative water system in addition to containing polymer gelling agent can also contain fire-extinguishing materials, such as alkali metal halides and diammonium phosphates and foaming surface active materials, as well as inorganic fire-retardant materials, such as diatomaceous earth, attapulgite and kaolinite.
- fire-extinguishing materials such as alkali metal halides and diammonium phosphates and foaming surface active materials
- inorganic fire-retardant materials such as diatomaceous earth, attapulgite and kaolinite.
- the manner of preparing the ablative water system can introduce other materials into the system which are utilized for considerations having no relation to the fire combating characteristics of the system.
- certain solid water-swellable cross-linked polymeric materials used as gelling agents in the form of slurries using a liquid carrier.
- the polyacrylamide water-swellable cross-linked polymer gelling agents are usefully suspended in isopropyl alcohol or other suitable carrier and stored in slurry form for addition to water when it is desired to set up an ablative water system in fighting a fire.
- the ablative water system can contain other agents desired to promote its effective delivery to the point of use.
- agents can be admixed in the ablative water system which reduce the friction in the pipe in which the system is delivered to its point of use, thus increasing the flowability of the ablative water system.
- Materials such as poly(ethylene oxides) are particularly useful for this purpose.
- dispersion or emulsion of insoluble materials, and the rapid solution of soluble materials are enhanced by the addition of surfactants.
- surfactants are sometimes found as components in ablative water systems for this purpose.
- surfactants have been utilized in combination with ablative water, that is in admixture or solution therein, as foaming agents to provide fire-extinguishing effect or as dispersing or emulsifying agents for additives included in admixture with ablative water.
- foaming agents to provide fire-extinguishing effect
- dispersing or emulsifying agents for additives included in admixture with ablative water.
- aqueous surfactant solution applied separately from ablative water to increase the penetration of ablative water applied to combustible materials, both those which are burning and those which are to be protected, thereby reducing the overall ablative water requirements. This use of aqueous surfactant solutions is the subject of the present invention.
- the required amount of ablative water to combat a fire can be reduced and that more effective and rapid action in combating the fire can be obtained by first treating the fire, or more particularly, the combustible materials on fire and threatened by fire, with water containing a compatible surfactant, that is with a compatible aqueous surfactant solution which wets the surface of combustible materials which are threatened with fire and which are to be protected such that when the ablative water is subsequently applied the presence of surfactant on the surface of combustible materials aids in the rapid spreading of ablative water over the combustible materials and in the deep penetration of ablative water to where the fire is.
- the method of this invention is applicable with advantage to combating fire with ablative water whatever the mechanical technique of water application.
- the pretreatment of combustible materials with water containing a surfactant should be of sufficient duration to wet the combustible materials, but should be terminated before substantial pooling and runoff of water occurs such that when followed by application of ablative water there is just sufficient wetting action to assist in penetrating the combustible materials which are threatened by fire and which are to be protected and the ablative water is not induced further to run off.
- the exact timing of the pretreatment will, of course, vary from fire to fire, although normally in an automatic sprinkler system it is desirable to apply the pretreatment water with surfactant utilizing the same sprinkler system as is subsequently utilized to apply the ablative water system. In such an arrangement, with water pressures the same, the pretreatment time is typically on the order of about 5 minutes, but can vary considerably from that time.
- any surfactant can be utilized in the pretreatment water system which is compatible with the gelling agent and other components of the ablative water system which follows in terms of application to the combustible materials.
- Those surfactants which are particularly contemplated are preferably wetting agents having the capability of reducing the surface tension of the water and desirably should be stable at temperatures at least up to the boiling point of water in order that they remain on the combustible surface to which applied while still wet.
- Suitable surfactants are, for example, nonionic organic detergents. Ionic surfactants, such as anionic or cationic detergents, are not suitable since such surfactants are not compatible with the gelling agent component of the subsequently applied ablative water since on contact with ablative water they act to destroy the ablative nature of the ablative water.
- Nonionic organic detergents suitable for use herein include, for example, polyethylene oxide condensates of alkylphenols where in the alkyl group contains from eight to 15 carbon atoms (e.g., t-octylphenol) and the ethylene oxide is present in a molar ratio of.
- ethylene oxide to alkylphenol in the range of 8:1 to 20:1; condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine wherein the molecular weight of the condensation products ranges from 5,000 to 11,000; the condensation products of from about 5 to 30 moles of ethylene oxide with one mole of a straight or branched chain aliphatic alcohol containing from eight to 18 carbon atoms, e.g., condensation product of 6 moles of ethylene oxide with one mole of lauryl alcohol; higher alkyl di-lower alkyl amine or phosphine oxides, e.g., dodecyldimethylamine oxide or dodecyldimethyl phosphine oxide; alkyl methyl sulfoxides such as dodecyl methyl sulfoxide.
- Preferred nonionic detergents for use herein are the polyoxyethylenated alkylphenols described above.
- Nozzles 13 can be any nozzles typically used in automatic sprinkler systems and are usually provided with a fusible link in a conventional manner, such that upon the temperature at the location of the nozzle reaching a predetermined maximum, the fusible link abruptly melts, opening a connection between the nozzles 13 and line 11 to permit water to flow from main 12 through nozzles 13 in a suitable spray pattern determined by the location of nozzles Line 11 adjacent main 12 is connected through lateral connections l4 and 15, respectively, to holding tanks 16 and 17.
- Each line 14 and 15 is provided with a normally closed, solenoid-operated valve, indicated by the reference numerals l8 and 19, respectively, which when actuated is operable to make connection between its respective holding tank 16 or 17 and line 11 through its associated line 14 or 15.
- each of lines 14 and 15 contains a suitable metering device, such as an orifice plate, such that flow through the line from its associated holding tank 16 or 17 is at a regulated rate when valve 18 or 19 is opened.
- a flow sensor device 20 is connected in line 11 and is operalble in response to flow through line 11, as occurs when nozzles 13 open, immediately to actuate valve 18 such that liquid contained in holding tank 16 is bled into the flowing stream in line ll.
- Sensor 20 also upon actuation in response to flow in line Ill immediately operates to actuate a time delay device 21 which in turn operates after a predetermined time delay to actuate valve 19 opening communication through line 15 between holding tank l7 and line 11 such that liquid in holding tank 17 is then metered into line 11.
- Time delay device 21 also responds on timing out to disconnect the operative circuit between sensor 20 and valve 18 to cause a valve 18 to close simultaneously with the opening of valve 19, thus discontinuing the flow of material from tank 16 into line 11 at the same time flow from tank 17 starts into line 11.
- holding tank 16 contains a premixed concentrated solution of water and surfactant.
- the surfactant can be Triton N-lOl, a proprietary product manufactured by Rohm & Haas Cov which is a polyethylene oxide condensate of nonyl phenol having about [2 to 13 moles ethylene oxide per mole of phenol.
- the Triton N-lOl is mixed in tank 16 with water on the basis, for example, of five parts by weight of Triton N-lOl with 100 parts by weight of water, and line 14 is adapted to meter liquid from tank 16 at the rate of one volume per 100 volumes of water in line 11.
- the gelling agent can be a commercially available polyacrylamide sold under the trade name Gelgard" referred to hereinbefore, In preparing the premix of the gelling agent for storage in holding tank 17 the Gelgard which is a solid particulate material is slurried at the rate of i140 pounds per barrel of isopropyl alcohol tone barrel isopropyl alcohol equals 354 pounds net).
- the metering rate of liquid through line 15 should be adjusted to mix the slurry in tank 17 with water in line 11 to set up a gel. Normally the thickening agent, Gelgard, illustrated sets best at l3 pounds per gallons of water.
- Time delay device 21 is preset in accordance with the design considerations of the particular sprinkler system 10 and typically is preset to time out after 5 minutes. The preset timing of time delay device 21 should be set such that the water-containing surfactant being delivered through nozzles 13 to the fire is sufficient to cause penetration of the tire by the surfactant solution deep into the fire without excess to the extent that water pools or runs off.
- the action of the fire causes the water to boil off at the hottest points, but leaves those combustible surfaces not yet burning or overheated relatively wet such that when time delay device 21 times out to introduce the gelling agent from holding tank 17 to line 11 and to discontinue the flow of surfactant from holding tank 15, the ablative water system formed by the addition of gelling agent to the water in line 11 which is then delivered to the fire slides rapidly over the combustible materials which remain wet to the point where the fire has dried, thus piling up ablative water at the location of the tire itself where its action is most effecme.
- ablative water is required with respect to a water-repellent surface, such as the surface of a stack of rubber tires
- Such coextensive application can be carried out utilizing two automatic sprinkler systems, one to apply ablative water and the other to apply aqueous surfactant solution.
- a method of combating fire upon an indication of the occurrence of fire among combustible materials which comprises, applying to said materials an aqueous nonionic organic surfactant solution which is compatible with ablative water so as to wet the surface of said materials and thereafter applying to said combustible materials an ablative water system whereby the penetration and coverage of said ablative water is increased.
- said surfactant is a polyethylene oxide condensate of alkylphenol wherein the alkyl group contains from eight to 15 carbon atoms and the ethylene oxide is present in a molar ratio of ethylene oxide to alkylphenol in the range of 8:1 to 20:].
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Abstract
The application of ablative water in combating fire is improved by wetting the surfaces of the combustible materials to be protected with water containing a surfactant prior to the application of ablative water to such surfaces in order that the subsequently applied ablative water readily penetrates the combustible material down to where the fire is in order that the ablative water be available where it is required.
Description
United States Patent 1151 3,647,001
Livingston 1 Mar. 7, 1972 54] COMBATING FIRE WITH ABLATIVE 3,229,769 1/1966 Bashaw et a1. ..l69/1 WATER 3,247,171 4/1966 Walker et a]. ..260/80.3
3,345,289 10/1967 Freifeldetal ....252/8.l 1 lnvemofi Willwm h-LivinaswmNorwwdMass- 3,354,084 11/1967 Katzer .252/2 [73] Assignee: Factory Mutual Research Corporation,
Boston-Providence Turnpike, Mass. Pfima'y Examinerjohn Goolkasian Assistant Examiner-D. J. Fritsch [22] Filed: Apr. 22, 1970 Attorney-Lane, Aitken, Dunner 81 Ziems [21] Appl. No.: 30,835 [57] ABSTRACT The application of ablative water in combating fire is im- [52] US. CL ..l69/l A, 169/ 1 B, 169/14, proved by wetting the Surfaces f h combustible materials to 252/21 252/8-05 be protected with water containing a surfactant prior to the [5 I] Int. Cl. ..A62 1/06, A62d l/UO p li ti of blative water to such surfaces in order that the [58] Field of Search "252/2, 3, 8.05, 315, 316; subsequently applied ablative water readily penetrates the 169/1 l l 14 combustible material down to where the tire is in order that the ablative water be available where it is required.
[56] References Cited 2 Claims, 1 Drawing Figure UNITED STATES PATENTS CONCv SOL'NDF GELLING AGENT SURFACTANT CARRIER WATER MAIN 12 14 11 15 FUSIBLE LINK 13 COMBATING FIRE WITH ABLATIVE WATER BACKGROUND OF THE INVENTION This invention is directed to the field of combating fires utilizing ablative fluid material systems.
An ablative material as comprehended within the present invention is a material which, when present in a layer of sufficient thickness, will permit thermal energy to be transmitted through its exposed outer surface but not completely through said layer, said thermal energy being absorbed within said layer so as to immediately transform the material of said layer into vapor without internal convection of said material, said vapor leaving said layer through its outer surface.
The use of an ablative fluid material to combat a fire in a building or other confined location by the application of, said material from an automatically operable fixed source such as an automatic sprinkler system is described in commonly assigned patent application of Livingston et al. Ser. No. 766,475 filed Oct. 10, 1968.
As described in the aforementioned Livingston et al. application water is converted to an ablative fluid material by the admixture therewith of a water-swellable cross-linked polymer. The formed ablative fluid material is in the form of a gel and is denoted ablative water.
Water-swellable cross-linked polymers useful as gelling agents to convert water to ablative water are described in Katzer U.S. Pat. No. 3,354,084 and Bashaw et al. U.S. Pat. No. 3,229,769. One useful water-swellable cross-linked polymer is sold by B. F. Goodrich Chemical Company under the designation Carbopol-960. Another useful water-swellable cross-linked polymer is sold by Dow Chemical under the designation of Gelgard M. Gelgard M is described in my copending application Ser. No. 13,179 filed Feb. 20, 1970 titled Slurry Additive for Ablative Water Fire Extinguishing Systems.
The ablative water system in addition to containing polymer gelling agent can also contain fire-extinguishing materials, such as alkali metal halides and diammonium phosphates and foaming surface active materials, as well as inorganic fire-retardant materials, such as diatomaceous earth, attapulgite and kaolinite. Generally speaking the choice of gelling agent and other fire retardant materials added will be dictated by con siderations having no relevance to this invention.
In addition the manner of preparing the ablative water system can introduce other materials into the system which are utilized for considerations having no relation to the fire combating characteristics of the system. Thus for example in automatic sprinkler systems it is desirable to premix certain solid water-swellable cross-linked polymeric materials used as gelling agents in the form of slurries using a liquid carrier. For example the polyacrylamide water-swellable cross-linked polymer gelling agents are usefully suspended in isopropyl alcohol or other suitable carrier and stored in slurry form for addition to water when it is desired to set up an ablative water system in fighting a fire. Furthermore the ablative water system can contain other agents desired to promote its effective delivery to the point of use. For example agents can be admixed in the ablative water system which reduce the friction in the pipe in which the system is delivered to its point of use, thus increasing the flowability of the ablative water system. Materials such as poly(ethylene oxides) are particularly useful for this purpose. Similarly the dispersion or emulsion of insoluble materials, and the rapid solution of soluble materials are enhanced by the addition of surfactants. Surfactants are sometimes found as components in ablative water systems for this purpose.
Thus, surfactants have been utilized in combination with ablative water, that is in admixture or solution therein, as foaming agents to provide fire-extinguishing effect or as dispersing or emulsifying agents for additives included in admixture with ablative water. Heretofore, it has not been known to utilize an aqueous surfactant solution applied separately from ablative water to increase the penetration of ablative water applied to combustible materials, both those which are burning and those which are to be protected, thereby reducing the overall ablative water requirements. This use of aqueous surfactant solutions is the subject of the present invention.
SUMMARY OF THE INVENTION In accordance with the present invention it has been found that the required amount of ablative water to combat a fire can be reduced and that more effective and rapid action in combating the fire can be obtained by first treating the fire, or more particularly, the combustible materials on fire and threatened by fire, with water containing a compatible surfactant, that is with a compatible aqueous surfactant solution which wets the surface of combustible materials which are threatened with fire and which are to be protected such that when the ablative water is subsequently applied the presence of surfactant on the surface of combustible materials aids in the rapid spreading of ablative water over the combustible materials and in the deep penetration of ablative water to where the fire is. The method of this invention is applicable with advantage to combating fire with ablative water whatever the mechanical technique of water application.
In accordance with this invention the pretreatment of combustible materials with water containing a surfactant should be of sufficient duration to wet the combustible materials, but should be terminated before substantial pooling and runoff of water occurs such that when followed by application of ablative water there is just sufficient wetting action to assist in penetrating the combustible materials which are threatened by fire and which are to be protected and the ablative water is not induced further to run off. The exact timing of the pretreatment will, of course, vary from fire to fire, although normally in an automatic sprinkler system it is desirable to apply the pretreatment water with surfactant utilizing the same sprinkler system as is subsequently utilized to apply the ablative water system. In such an arrangement, with water pressures the same, the pretreatment time is typically on the order of about 5 minutes, but can vary considerably from that time.
Generally any surfactant can be utilized in the pretreatment water system which is compatible with the gelling agent and other components of the ablative water system which follows in terms of application to the combustible materials. Those surfactants which are particularly contemplated are preferably wetting agents having the capability of reducing the surface tension of the water and desirably should be stable at temperatures at least up to the boiling point of water in order that they remain on the combustible surface to which applied while still wet.
Suitable surfactants are, for example, nonionic organic detergents. Ionic surfactants, such as anionic or cationic detergents, are not suitable since such surfactants are not compatible with the gelling agent component of the subsequently applied ablative water since on contact with ablative water they act to destroy the ablative nature of the ablative water.
Nonionic organic detergents suitable for use herein include, for example, polyethylene oxide condensates of alkylphenols where in the alkyl group contains from eight to 15 carbon atoms (e.g., t-octylphenol) and the ethylene oxide is present in a molar ratio of. ethylene oxide to alkylphenol in the range of 8:1 to 20:1; condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylene diamine wherein the molecular weight of the condensation products ranges from 5,000 to 11,000; the condensation products of from about 5 to 30 moles of ethylene oxide with one mole of a straight or branched chain aliphatic alcohol containing from eight to 18 carbon atoms, e.g., condensation product of 6 moles of ethylene oxide with one mole of lauryl alcohol; higher alkyl di-lower alkyl amine or phosphine oxides, e.g., dodecyldimethylamine oxide or dodecyldimethyl phosphine oxide; alkyl methyl sulfoxides such as dodecyl methyl sulfoxide.
ll,647.00l
Preferred nonionic detergents for use herein are the polyoxyethylenated alkylphenols described above.
BRIEF DESCRIPTION OF THE DRAWING For a more complete understanding of the practical application of this invention, reference is made to the appended drawing which illustrates a flowsheet of an automatic sprinkler system utilized in carrying out this invention,
DETAILED DESCRIPTION OF THE INVENTION In the drawing the reference numeral generally designates a sprinkler system including line 11 connected at one end of a water main l2 and leading to outlet nozzles 13 lonly one is shown). Nozzles 13 can be any nozzles typically used in automatic sprinkler systems and are usually provided with a fusible link in a conventional manner, such that upon the temperature at the location of the nozzle reaching a predetermined maximum, the fusible link abruptly melts, opening a connection between the nozzles 13 and line 11 to permit water to flow from main 12 through nozzles 13 in a suitable spray pattern determined by the location of nozzles Line 11 adjacent main 12 is connected through lateral connections l4 and 15, respectively, to holding tanks 16 and 17. Each line 14 and 15 is provided with a normally closed, solenoid-operated valve, indicated by the reference numerals l8 and 19, respectively, which when actuated is operable to make connection between its respective holding tank 16 or 17 and line 11 through its associated line 14 or 15. In addition each of lines 14 and 15 contains a suitable metering device, such as an orifice plate, such that flow through the line from its associated holding tank 16 or 17 is at a regulated rate when valve 18 or 19 is opened.
A flow sensor device 20 is connected in line 11 and is operalble in response to flow through line 11, as occurs when nozzles 13 open, immediately to actuate valve 18 such that liquid contained in holding tank 16 is bled into the flowing stream in line ll. Sensor 20 also upon actuation in response to flow in line Ill immediately operates to actuate a time delay device 21 which in turn operates after a predetermined time delay to actuate valve 19 opening communication through line 15 between holding tank l7 and line 11 such that liquid in holding tank 17 is then metered into line 11. Time delay device 21 also responds on timing out to disconnect the operative circuit between sensor 20 and valve 18 to cause a valve 18 to close simultaneously with the opening of valve 19, thus discontinuing the flow of material from tank 16 into line 11 at the same time flow from tank 17 starts into line 11.
In operation holding tank 16 contains a premixed concentrated solution of water and surfactant. For example the surfactant can be Triton N-lOl, a proprietary product manufactured by Rohm & Haas Cov which is a polyethylene oxide condensate of nonyl phenol having about [2 to 13 moles ethylene oxide per mole of phenol. In such case the Triton N-lOl is mixed in tank 16 with water on the basis, for example, of five parts by weight of Triton N-lOl with 100 parts by weight of water, and line 14 is adapted to meter liquid from tank 16 at the rate of one volume per 100 volumes of water in line 11.
In a typical installation the gelling agent can be a commercially available polyacrylamide sold under the trade name Gelgard" referred to hereinbefore, In preparing the premix of the gelling agent for storage in holding tank 17 the Gelgard which is a solid particulate material is slurried at the rate of i140 pounds per barrel of isopropyl alcohol tone barrel isopropyl alcohol equals 354 pounds net). Added to this mixture in holding tank 17 are 1,000 mlv Polyox FRA" *{Polyox lFRA is a high molecular weight poly(ethyleneoxide) sold by Union Carbide Corporation.) per barrel of isopropyl alcohol to reduce the friction of flow in pipe 11 and through nozzles l3 when the mixture in holding tank 17 is introduced to pipe 11. In accordance with William L. Livingston copending application filed concurrently herewith titled "Preparation of \blative Water" there is also added to the material in holdin tank 17, 20 pounds per barrel of isopropyl alcohol of Cab-o-sfi M-S, a proprietary product which is a colloidal pyrogenic silica having a surface area of 200 square meters per gram and sold by Cabot Corporation and which in accordance with the above copending application functions to stabilize the slurry in holding tank 17 to permit its storage without agitation for substantial periods of time, i.e., 6 months to a year. The metering rate of liquid through line 15 should be adjusted to mix the slurry in tank 17 with water in line 11 to set up a gel. Normally the thickening agent, Gelgard, illustrated sets best at l3 pounds per gallons of water.
In accordance with the invention when a fire occurs at the location of any of nozzles 13 causing their fusible links to abruptly melt and permitting flow through them, the consequent flow of water in pipe 11 actuates sensor 20 immediately actuating valve 18 such that the concentrated surfactant solution in holding tank 15 is bled into line 11 to produce a concentration of the surfactant on the order of 0.05 weight percent. Time delay device 21 is preset in accordance with the design considerations of the particular sprinkler system 10 and typically is preset to time out after 5 minutes. The preset timing of time delay device 21 should be set such that the water-containing surfactant being delivered through nozzles 13 to the fire is sufficient to cause penetration of the tire by the surfactant solution deep into the fire without excess to the extent that water pools or runs off. The action of the fire causes the water to boil off at the hottest points, but leaves those combustible surfaces not yet burning or overheated relatively wet such that when time delay device 21 times out to introduce the gelling agent from holding tank 17 to line 11 and to discontinue the flow of surfactant from holding tank 15, the ablative water system formed by the addition of gelling agent to the water in line 11 which is then delivered to the fire slides rapidly over the combustible materials which remain wet to the point where the fire has dried, thus piling up ablative water at the location of the tire itself where its action is most effecme.
Where better coverage of ablative water is required with respect to a water-repellent surface, such as the surface of a stack of rubber tires, it can be desirable to apply separate streams of aqueous compatible surfactant solution and ablative water to said surface at the same time whereby more of said surface is provided with a thicker layer of ablative water. Such coextensive application can be carried out utilizing two automatic sprinkler systems, one to apply ablative water and the other to apply aqueous surfactant solution.
The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.
What is claimed is:
l. A method of combating fire upon an indication of the occurrence of fire among combustible materials which comprises, applying to said materials an aqueous nonionic organic surfactant solution which is compatible with ablative water so as to wet the surface of said materials and thereafter applying to said combustible materials an ablative water system whereby the penetration and coverage of said ablative water is increased.
2. A method as described in claim 1 wherein said surfactant is a polyethylene oxide condensate of alkylphenol wherein the alkyl group contains from eight to 15 carbon atoms and the ethylene oxide is present in a molar ratio of ethylene oxide to alkylphenol in the range of 8:1 to 20:].
Claims (1)
- 2. A method as described in claim 1 wherein said surfactant is a polyethylene oxide condensate of alkylphenol wherein the alkyl group contains from eight to 15 carbon atoms and the ethylene oxide is present in a molar ratio of ethylene oxide to alkylphenol in the range of 8:1 to 20:1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3083570A | 1970-04-22 | 1970-04-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3647001A true US3647001A (en) | 1972-03-07 |
Family
ID=21856294
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US30835A Expired - Lifetime US3647001A (en) | 1970-04-22 | 1970-04-22 | Combating fire with ablative water |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3647001A (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3739794A (en) * | 1971-09-10 | 1973-06-19 | Gelco Project Lindgren & Co | Method and apparatus for continuously preparing a gel |
| US3831617A (en) * | 1971-11-02 | 1974-08-27 | Factory Mutual Res Corp | Additive injection system |
| US3888641A (en) * | 1972-07-24 | 1975-06-10 | Nittan Co Ltd | Method of erasing smoke |
| US4526234A (en) * | 1983-10-21 | 1985-07-02 | Little Ralph V | Wetting agent injection system |
| US5945026A (en) * | 1994-11-04 | 1999-08-31 | Hazard Control Technologies, Inc. | Composition and methods for firefighting hydrocarbon fires |
| US6139775A (en) * | 1994-11-04 | 2000-10-31 | Hazard Control Technologies, Inc. | Compositions and methods for treating hydrocarbon materials |
| US6371384B1 (en) * | 2000-05-16 | 2002-04-16 | The United States Of America As Represented By The Secretary Of The Navy | Aqueous foam generating system and method for generating foam having long wet-to-dry transition times |
| US6386293B1 (en) * | 2000-05-09 | 2002-05-14 | John B. Bartlett | Fire combating system and method |
| WO2006013180A1 (en) * | 2004-08-02 | 2006-02-09 | Watermist-Systems Gmbh & Co. Kg | Extinguishing system and method for preventing and/or reducing smoke and/or fire from spreading |
| US20160030791A1 (en) * | 2014-08-01 | 2016-02-04 | Leonard E. Doten | Aircraft water tank polymer gel preparation system |
| WO2016082004A1 (en) * | 2014-11-28 | 2016-06-02 | Ofb Fire Solutions Pty Ltd | Fire-fighting system |
| US20160279451A1 (en) * | 2014-08-01 | 2016-09-29 | Leonard E. Doten | Aircraft firefighting tank with mixing |
| US20160325128A1 (en) * | 2015-05-06 | 2016-11-10 | Black Peak Laboratory LLC | Aqueous film-forming foam fire fighting system, method and apparatus |
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| US3229769A (en) * | 1963-01-28 | 1966-01-18 | Dow Chemical Co | Method for controlling the spread of fire |
| US3247171A (en) * | 1963-04-08 | 1966-04-19 | Dow Chemical Co | Process for hydrolyzing a cross-linked acrylamide polymer and the product thereby |
| US3345289A (en) * | 1965-11-01 | 1967-10-03 | Gen Aniline & Film Corp | Fire retardant composition of diammonium phosphate containing methylvinyl ether-maleic anhydride copolymer as thickener |
| US3354084A (en) * | 1964-06-24 | 1967-11-21 | Dow Chemical Co | Aqueous gel of water-swellable acrylic polymer and non-ionic filler |
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| US3229769A (en) * | 1963-01-28 | 1966-01-18 | Dow Chemical Co | Method for controlling the spread of fire |
| US3247171A (en) * | 1963-04-08 | 1966-04-19 | Dow Chemical Co | Process for hydrolyzing a cross-linked acrylamide polymer and the product thereby |
| US3480546A (en) * | 1964-02-28 | 1969-11-25 | Dow Chemical Co | Aqueous foam containing a waterswellable polymer flameproofing composition and process of making same |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3739794A (en) * | 1971-09-10 | 1973-06-19 | Gelco Project Lindgren & Co | Method and apparatus for continuously preparing a gel |
| US3831617A (en) * | 1971-11-02 | 1974-08-27 | Factory Mutual Res Corp | Additive injection system |
| US3888641A (en) * | 1972-07-24 | 1975-06-10 | Nittan Co Ltd | Method of erasing smoke |
| US4526234A (en) * | 1983-10-21 | 1985-07-02 | Little Ralph V | Wetting agent injection system |
| US5945026A (en) * | 1994-11-04 | 1999-08-31 | Hazard Control Technologies, Inc. | Composition and methods for firefighting hydrocarbon fires |
| US6139775A (en) * | 1994-11-04 | 2000-10-31 | Hazard Control Technologies, Inc. | Compositions and methods for treating hydrocarbon materials |
| US6386293B1 (en) * | 2000-05-09 | 2002-05-14 | John B. Bartlett | Fire combating system and method |
| US6786286B1 (en) | 2000-05-09 | 2004-09-07 | Barricade International, Inc. | Fire combating system and method |
| US6371384B1 (en) * | 2000-05-16 | 2002-04-16 | The United States Of America As Represented By The Secretary Of The Navy | Aqueous foam generating system and method for generating foam having long wet-to-dry transition times |
| WO2006013180A1 (en) * | 2004-08-02 | 2006-02-09 | Watermist-Systems Gmbh & Co. Kg | Extinguishing system and method for preventing and/or reducing smoke and/or fire from spreading |
| US20160030791A1 (en) * | 2014-08-01 | 2016-02-04 | Leonard E. Doten | Aircraft water tank polymer gel preparation system |
| US20160279451A1 (en) * | 2014-08-01 | 2016-09-29 | Leonard E. Doten | Aircraft firefighting tank with mixing |
| US9656108B2 (en) * | 2014-08-01 | 2017-05-23 | Leonard E. Doten | Aircraft water tank polymer gel preparation system |
| US10195471B2 (en) * | 2014-08-01 | 2019-02-05 | Leonard E. Doten | Aircraft firefighting tank with mixing |
| US10940344B2 (en) | 2014-08-01 | 2021-03-09 | Leonard E. Doten | Firefighting polymer gel preparation onboard aircraft |
| US10940343B2 (en) | 2014-08-01 | 2021-03-09 | Leonard E. Doten | Firefighting polymer gel preparation onboard aircraft |
| US10940342B2 (en) | 2014-08-01 | 2021-03-09 | Leonard E. Doten | Firefighting polymer gel preparation onboard aircraft |
| US10940345B2 (en) | 2014-08-01 | 2021-03-09 | Leonard E. Doten | Firefighting polymer gel preparation onboard aircraft |
| WO2016082004A1 (en) * | 2014-11-28 | 2016-06-02 | Ofb Fire Solutions Pty Ltd | Fire-fighting system |
| US20170259091A1 (en) * | 2014-11-28 | 2017-09-14 | Ofb Fire Solutions Pty Ltd | Fire-fighting system |
| US20160325128A1 (en) * | 2015-05-06 | 2016-11-10 | Black Peak Laboratory LLC | Aqueous film-forming foam fire fighting system, method and apparatus |
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