US3849315A - Film-forming fire fighting composition - Google Patents

Film-forming fire fighting composition Download PDF

Info

Publication number
US3849315A
US3849315A US00254404A US25440472A US3849315A US 3849315 A US3849315 A US 3849315A US 00254404 A US00254404 A US 00254404A US 25440472 A US25440472 A US 25440472A US 3849315 A US3849315 A US 3849315A
Authority
US
United States
Prior art keywords
liquid
fire
fighting
percent
foamability
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US00254404A
Inventor
P Chiesa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NAT FOAM SYST Inc
NAT FOAM SYST INC US
Kidde Fire Fighting Inc
Original Assignee
NAT FOAM SYST Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US00254404A priority Critical patent/US3849315A/en
Application filed by NAT FOAM SYST Inc filed Critical NAT FOAM SYST Inc
Priority to JP47086735A priority patent/JPS5233920B2/ja
Priority to AU55172/73A priority patent/AU470208B2/en
Priority to GB2354873A priority patent/GB1431982A/en
Priority to CA171,787A priority patent/CA994539A/en
Publication of US3849315A publication Critical patent/US3849315A/en
Application granted granted Critical
Priority to US05/525,175 priority patent/US4038195A/en
Priority to US05/670,252 priority patent/US4060489A/en
Assigned to ENTERRA CORPORATION reassignment ENTERRA CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: PHILADELPHIA SUBURBAN CORPORATION
Assigned to NATIONAL FOAM SYSTEM, INC. reassignment NATIONAL FOAM SYSTEM, INC. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: ENTERRA CORPORATION
Assigned to CHUBB NATIONAL FOAM, INC. reassignment CHUBB NATIONAL FOAM, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). EFFECTIVE DATE MAY 31, 1988 Assignors: NATIONAL FOAM SYSTEM, INC.
Assigned to CHUBB NATIONAL FOAM, INC. reassignment CHUBB NATIONAL FOAM, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). MAY 31, 1988, PENNSYLVANIA Assignors: NATIONAL FOAM SYSTEM, INC.
Assigned to NATIONAL FOAM SYSTEM, INC., A PA CORP. reassignment NATIONAL FOAM SYSTEM, INC., A PA CORP. RECORD TO DELETE PATENT NUMBERS ERRONEOUSLY LISTED ON (SEE EXHIBIT 3) AND RECORDED AT REEL 4760 FRAMES 0317 ETC. ON JUNE 22, 1987. ASSIGNOR HEREBY ASSIGNS THE ENTIRE INTEREST EFFECTIVE OCTOBER 03, 1990. SEE RECORD FOR DETAILS Assignors: ENTERRA CORPORATION
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D1/00Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
    • A62D1/0071Foams
    • A62D1/0085Foams containing perfluoroalkyl-terminated surfactant
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/905Agent composition per se for colloid system making or stabilizing, e.g. foaming, emulsifying, dispersing, or gelling
    • Y10S516/906The agent contains organic compound containing silicon
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/905Agent composition per se for colloid system making or stabilizing, e.g. foaming, emulsifying, dispersing, or gelling
    • Y10S516/914The agent contains organic compound containing nitrogen, except if present solely as NH4+

Definitions

  • ABSTRACT Aqueous foam film-forming fire fighting compositions based on mixtures of fluorocarbon and siloxane surfactants, are improved for sub-surface introduction into burning hydrophobic liquids by the addition of a different surfactant that increases foamability and has a hydrophilic moiety weighing at least 80 percent more than its lipophilic moiety.
  • the present invention relates to fire fighting, and particularly to the use of film-formingcompositions in the fighting of fires.
  • aqueous film-forming liquid containing dissolved fluorocarbon and silicone surfactants in amounts that give the liquid a surface tension at least as low as 19 dynes per centimeter but do not give it good foamability
  • improvement is made pursuant to the present invention by having the liquid also contain a different surfactant that has a hydrophilic moiety whose weight is at least 80 percent greater and more desirably at least 120 percent greater than its lipophilic moiety, and is contained in an amount at least about 40 percent of that which provides good foamability to the liquid.
  • Preferred lipophilic moieties for the last mentioned surfactant are hydrocarbon chains not over 10 carbons long, or betterstill only 7 0r 8 carbons long. Also the best hydrophilic moieties contain at least 3 hydrophile units such as hydroxyl, carboxyl, sulfo and nitrogen. Particularly effective surfactants are those of the imidazoline type containing a quaternized nitrogen hydroxide carrying two short carboxylated chains. Others falling within the foregoing definition and providing very good results include disodium n-octyl amine dipropionate.
  • a feature of the present invention is that the firefighting foams thus produced are very effective for extinguishing fires in burning hydrophobic liquids by introducing the foam into the burning liquid below the liquids surface.
  • Such sub-surface introduction is a particularly desirable technique for fighting fires in storage tanks, for example, inasmuch as less vulnerable and less expensive foam-supplying installations can be used.
  • the fire-fighting composition of the present invention can also contain other ingredients such as antifreeze agents, hydrophilic resins, buffers, sequestering agents such as those for the cations of sea water, preservatives, the acetylene glycols of Ser. No. 131,763, etc.
  • the new composition can also be prepared from concentrates which are diluted with tap or sea water when needed to be applied to a'fire.
  • the foregoing ingredients are mixed in any order and the final product is a so-called 6 percent fire-fighting concentrate. It can be stored for many months, and is used for fire-fighting by mixing it with 16% times its volume of water and also with sufficient air to foam with an expension of 3 to 6. This expansion is generally considered adequate for fire fighting.
  • Such mixing is conveniently effected with a high-back-pressure venturi as shown in US. Pat. No. 3,475,333 granted Oct. 28, 1969, for sub-surface introduction into the usual types of storage tanks.
  • This mixture can be used interchangeably with that of Example I, but by reason of the sequestering action of the nitrilotriacetate it works better than that of Example I when diluted with sea water.
  • the silicone surfactant is somewhat more stable in a solution that contains isopropyl alcohol. It is accordingly helpful to increase the amount of isopropyl alcohol in the 6 percent concentrates of Examples I and II. As much as percent by weight isopropyl alcohol can thus be present in those concentrates. Larger concentrations are undesirable inasmuch as they tend to unduly lower the flash point of the concentrates.
  • the silicone surfactants are also more stable if kept from acid media and as in Ser. No. l3l,763 a pH of about 7.8 is preferred for the concentrates of the present invention.
  • the tris hydroxymethylamino methane helps buffer the concentrates of the foregoing Examples at about that pH, even when they are mixed with other concentrates that are acid.
  • fluorocarbon surfactants disclosed in Ser. No. 131,763 can be used in place of those of Examples l and Il.
  • Other anionic, cationic or amphoteric fluocarbon surfactants such as those shown to be effective in U.S. Pat. No. 3,655,555, granted Apr. ll, 1972, can also be so used.
  • any of the silicone surfactants of that prior application can be used in place of those of Examples l and II.
  • a fungicide such as formaldehyde or the sodium salt of o-phenyl-phenol can also be added to the concentrates to inhibit mold growth and the like.
  • the concentrates of the present invention can also be prepared for dilution in proportions other than the 1655:] ratio given above. Another widely used dilution ratio is 33 18:] and for such use the concentrates can be prepared to have double the strength shown in Examples I and II. Other dilutions take correspondingly modified concentrates, although it is not necessary to accurately proportion the dilution. As much as a plus or minus 50 percent departure from the target dilution proportion can be tolerated. One reason for such tolerance is that the fire-fighting effectiveness of the diluted mixtures is not dependent to any significant degree on good foaming. Even a foam of the present invention with an expansion of 2 will do a good job of rapidly extinguishing a gasoline fire by subsurface introduction.
  • the imidazoline surfactant is so effective that it is diluted with more than an equal amount of less effective surfactant composition outside the scope of the present invention. That example can be substantially improved by replacing the less effective surfactant composition by an additional quantity of the imidazoline surfactant of Examples I or ,II, or any other imidazoline surfactant such as
  • the long unsubstituted alkyl chain of 7 to 9 carbons is the lipophilic moiety.
  • the balance of the molecule is the hydrophilic moiety and contains a multiplicity of hydrophile units.
  • the quaternary hydroxylated nitrogen is one such unit, the other nitrogen is a second, and the alcohol, carboxy and sulfo groups are additional ones.
  • a chain of two carbons will not detract from the hydrophilic character even if such chain is fully hydrogenated and also carries a methyl branch. Oxygen or nitrogens should therefore interrupt carbon chains to leave chain lengths not more than two carbons long.
  • the two carbons connected together in the imidazoline ring are counted as part of the hydrophilic moiety, as is the CH CH OCH portion of the imidazoline of Example 1.
  • the ring carbon to which the lipophilic moiety is connected has two nitrogens also directly connected to it and for that reason is considered part of the hydrophilic moiety.
  • n-octyl amine di-propionic acid e.g., C H, N(CH CH COONa) or the corresponding salts of n-octyl amine di-2-methyl propionic acid although they are somewhat less effective. Because of the prohibitive expense it is impractical to use a fluorocarbon or siloxane type surfactant as a foamabilityimproving material.
  • aqueous film-forming fire-fighting foamable liquid containing dissolved fluorocarbon and silicone surfactants in amounts that give the liquid a surface tension at least as low as 19 dynes per centimeter but do not give it good foamability and also containing one or more foamability-increasing surfactants that are neither fluorocarbons nor silicones, to bring the foamability of the liquid up to the level needed for a fire-fighting foam
  • the improvement according to which at least 40 percent of the foamability-increasing surfactants is an imidazoline or amine di-propionate surfactant with hydrophilic and lipophilic moieties of which the hydrophilic moiety has at least three hydrophile units selected from the class consisting of hydroxyl, carboxyl, sulfo and nitrogen, and weighs at least 80 percent more than the lipophilic moiety.
  • R is a C to C alkyl
  • the amine dipropionate surfactant is C H N(CH CH COONa) or '6.

Abstract

Aqueous foam film-forming fire fighting compositions based on mixtures of fluorocarbon and siloxane surfactants, are improved for sub-surface introduction into burning hydrophobic liquids by the addition of a different surfactant that increases foamability and has a hydrophilic moiety weighing at least 80 percent more than its lipophilic moiety.

Description

[451 Nov. 19, 1974 1 FILM-FORMING FIRE FIGHTING COMPOSITION [75] Inventor: Peter Jordan Chiesa, Jr., Penn Township, Chester County, Pa.
[73] Assigneez National Foam System, Inc., West Chester, Pa. I
[22] Filed: May 18, 1972 [21] Appl. No.: 254,404
[52] US. Cl 252/3, 252/8.05, 252/307, 252/310, 252/311-312, 260/4482 R, 260/4682 N [51] Int. Cl A6211 l/00 [58] Field of Search 252/3, 8.05, 307, 310, 252/311-312, 357; 260/4482 R, 448.2 N, 260/3096 [56] References Cited UNITED STATES PATENTS 2,781,387 2/1957 Mannheimer 260/3096 2,875,210 2/1959 Bollenback et a1. 252/357 3,257,407 6/1966 Brace 252/8.05 3,475,333 10/1969 Meldray et a1... 252/3 3,531,417 9/1970 Morehouse 252/312 3,531,507 9/1970 Morehouse... 260/4482 3,562,156 2/1971 Francen 252/8.05 3,621,917 11/1971 Rosen et a1. 2'52/3 x 3,655,555 4/1972 Rossmy et al.,.,. 252/3 3,661,776 5/1972 Fletcher at 211.... 252/3 3,677,347 7/1972 Rosen et a1. 252/3 X Primary Examiner-Mayer Weinblatt Attorney, Agent, or Firm-Conno11y and Hutz [5 7] ABSTRACT Aqueous foam film-forming fire fighting compositions based on mixtures of fluorocarbon and siloxane surfactants, are improved for sub-surface introduction into burning hydrophobic liquids by the addition of a different surfactant that increases foamability and has a hydrophilic moiety weighing at least 80 percent more than its lipophilic moiety.
7 Claims, N0 Drawings The present invention relates to fire fighting, and particularly to the use of film-formingcompositions in the fighting of fires.
Application Ser. No. 131,763 filed Apr. 6, 1971, discloses aqueous foam compositions that spread films over hydrophobic liquids and in this way extinguish flames on such liquids. While those compositions do an admirable job in controlling fires in hydrophobic liquids, even when the foams do not cover the entire burning surface, one of the objects of the present invention is the provision of even more effective fire fighting filmforming compositions and methods.
The foregoing as well as additional objects of the present invention will be more completely understood from the following description of several of its exemplifications.
1t has been discovered that the fire-fighting compositions of application Ser. No. 131,763, the contents of which application are incorporated herein as though fully set forth, are improved by substituting for at least about 40 percent of the foam-ability-improving surfactant, one that has a hydrophilic moiety whose weight is at least 80 percent greater and better still at least 120 percent greater than the weight of its lipophilic moiety. In other words, in an aqueous film-forming liquid containing dissolved fluorocarbon and silicone surfactants in amounts that give the liquid a surface tension at least as low as 19 dynes per centimeter but do not give it good foamability, improvement is made pursuant to the present invention by having the liquid also contain a different surfactant that has a hydrophilic moiety whose weight is at least 80 percent greater and more desirably at least 120 percent greater than its lipophilic moiety, and is contained in an amount at least about 40 percent of that which provides good foamability to the liquid.
Preferred lipophilic moieties for the last mentioned surfactant are hydrocarbon chains not over 10 carbons long, or betterstill only 7 0r 8 carbons long. Also the best hydrophilic moieties contain at least 3 hydrophile units such as hydroxyl, carboxyl, sulfo and nitrogen. Particularly effective surfactants are those of the imidazoline type containing a quaternized nitrogen hydroxide carrying two short carboxylated chains. Others falling within the foregoing definition and providing very good results include disodium n-octyl amine dipropionate.
A feature of the present invention is that the firefighting foams thus produced are very effective for extinguishing fires in burning hydrophobic liquids by introducing the foam into the burning liquid below the liquids surface. Such sub-surface introduction is a particularly desirable technique for fighting fires in storage tanks, for example, inasmuch as less vulnerable and less expensive foam-supplying installations can be used.
The fire-fighting composition of the present invention can also contain other ingredients such as antifreeze agents, hydrophilic resins, buffers, sequestering agents such as those for the cations of sea water, preservatives, the acetylene glycols of Ser. No. 131,763, etc. The new composition can also be prepared from concentrates which are diluted with tap or sea water when needed to be applied to a'fire.
The following examples show typical compositions pursuant to the present invention.
EXAMPLE 1 55 grams (CF CF(CF ),,COO' NH C H where n is 4, a minor amount of which can be replaced by compounds where n is 2, 6 and 8,
128 grams of a 40 percent by weight solution in 1:1
by volume water-isopropanol, of
a minor amount of which can be replaced by compounds in which the bracketed portion occurs 2, 4 and 5 times, rather than three,
400 ml of a 48 percent by weight solution in water of 215 ml ofa 10 percent by weight solution in water of the condensation product of 3-dimethylaminopropylamine-l with an equivalent amount of an ethylene-maleic anhydride copolymer having 3 molar proportions of ethylene for every mol of maleic acid and having a viscosity of 7 cps. at normal pH as a 2 percent solution in water, a softening temperature of C. and a melting temperature of 235C. The condensation reaction which is slightly exothermic takes place in water solution at room temperature and opens each acid anhydride group to make one carboxyl and one amide of 3- dimethylamino-propylamine-l,
340 ml diethyleneglycol monobutyl ether,
20 g tris hydroxymethylamino methane, and
water to make 1 gallon.
The foregoing ingredients are mixed in any order and the final product is a so-called 6 percent fire-fighting concentrate. It can be stored for many months, and is used for fire-fighting by mixing it with 16% times its volume of water and also with sufficient air to foam with an expension of 3 to 6. This expansion is generally considered adequate for fire fighting. Such mixing is conveniently effected with a high-back-pressure venturi as shown in US. Pat. No. 3,475,333 granted Oct. 28, 1969, for sub-surface introduction into the usual types of storage tanks.
EXAMPLE I] 68 g of the fluorocarbon surfactant of Example I,
127 g of the same 40 percent solution of silicone surfactant described in Example I,
370 ml ethylene glycol,
467 ml of a 30 percent by weight aqueous solution of about a 1:1 mixture of sodium n-octyl and n-decyl sulfates,
467 ml of a 28 percent by weight aqueous solution of 31 g tris hydroxymethylamino methane,
6 g sodium nitrilotriacetate,
340 ml diethylene glycol monobutyl ether, and
water to make up 1 gallon.
This mixture can be used interchangeably with that of Example I, but by reason of the sequestering action of the nitrilotriacetate it works better than that of Example I when diluted with sea water.
The silicone surfactant is somewhat more stable in a solution that contains isopropyl alcohol. It is accordingly helpful to increase the amount of isopropyl alcohol in the 6 percent concentrates of Examples I and II. As much as percent by weight isopropyl alcohol can thus be present in those concentrates. Larger concentrations are undesirable inasmuch as they tend to unduly lower the flash point of the concentrates. The silicone surfactants are also more stable if kept from acid media and as in Ser. No. l3l,763 a pH of about 7.8 is preferred for the concentrates of the present invention. The tris hydroxymethylamino methane helps buffer the concentrates of the foregoing Examples at about that pH, even when they are mixed with other concentrates that are acid. There is however no need to preserve the pH when the concentrates are diluted for application to a fire inasmuch as the diluted fire-fighting liquid does not lose any significant fire-fighting ability if it is on the acid side for the relatively few minutes needed to control the fire.
Any of the fluorocarbon surfactants disclosed in Ser. No. 131,763 can be used in place of those of Examples l and Il. Other anionic, cationic or amphoteric fluocarbon surfactants such as those shown to be effective in U.S. Pat. No. 3,655,555, granted Apr. ll, 1972, can also be so used. Similarly any of the silicone surfactants of that prior application can be used in place of those of Examples l and II. A fungicide such as formaldehyde or the sodium salt of o-phenyl-phenol can also be added to the concentrates to inhibit mold growth and the like.
The concentrates of the present invention can also be prepared for dilution in proportions other than the 1655:] ratio given above. Another widely used dilution ratio is 33 18:] and for such use the concentrates can be prepared to have double the strength shown in Examples I and II. Other dilutions take correspondingly modified concentrates, although it is not necessary to accurately proportion the dilution. As much as a plus or minus 50 percent departure from the target dilution proportion can be tolerated. One reason for such tolerance is that the fire-fighting effectiveness of the diluted mixtures is not dependent to any significant degree on good foaming. Even a foam of the present invention with an expansion of 2 will do a good job of rapidly extinguishing a gasoline fire by subsurface introduction.
It will be noted that in the foregoing Example [I the imidazoline surfactant is so effective that it is diluted with more than an equal amount of less effective surfactant composition outside the scope of the present invention. That example can be substantially improved by replacing the less effective surfactant composition by an additional quantity of the imidazoline surfactant of Examples I or ,II, or any other imidazoline surfactant such as In the foregoing surfactants the long unsubstituted alkyl chain of 7 to 9 carbons is the lipophilic moiety. The balance of the molecule is the hydrophilic moiety and contains a multiplicity of hydrophile units. The quaternary hydroxylated nitrogen is one such unit, the other nitrogen is a second, and the alcohol, carboxy and sulfo groups are additional ones. A chain of two carbons will not detract from the hydrophilic character even if such chain is fully hydrogenated and also carries a methyl branch. Oxygen or nitrogens should therefore interrupt carbon chains to leave chain lengths not more than two carbons long. Thus the two carbons connected together in the imidazoline ring are counted as part of the hydrophilic moiety, as is the CH CH OCH portion of the imidazoline of Example 1. Similarly the ring carbon to which the lipophilic moiety is connected has two nitrogens also directly connected to it and for that reason is considered part of the hydrophilic moiety.
In place of the imidazoline type surfactant of Examples l and II there can be used the di-sodium, dipotassium or mixed sodium-potassium salt of n-octyl amine di-propionic acid, e.g., C H, N(CH CH COONa) or the corresponding salts of n-octyl amine di-2-methyl propionic acid although they are somewhat less effective. Because of the prohibitive expense it is impractical to use a fluorocarbon or siloxane type surfactant as a foamabilityimproving material.
Obviously many modifications and variations of the present invention are possible in the light of the above teachings. It is, therefore, to be understood that within the scope of the appended claims the invention may be practiced otherwise than as specifically described.
What is claimed is:
1. In an aqueous film-forming fire-fighting foamable liquid containing dissolved fluorocarbon and silicone surfactants in amounts that give the liquid a surface tension at least as low as 19 dynes per centimeter but do not give it good foamability and also containing one or more foamability-increasing surfactants that are neither fluorocarbons nor silicones, to bring the foamability of the liquid up to the level needed for a fire-fighting foam, the improvement according to which at least 40 percent of the foamability-increasing surfactants is an imidazoline or amine di-propionate surfactant with hydrophilic and lipophilic moieties of which the hydrophilic moiety has at least three hydrophile units selected from the class consisting of hydroxyl, carboxyl, sulfo and nitrogen, and weighs at least 80 percent more than the lipophilic moiety.
2. The combination of claim 1 in which the lipophilic moiety is in the form of a hydrocarbon chain not over carbons long.
3. The combination of claim 1 in which the imidazoline has one of its ring nitrogens quaternized with two carboxylated carbon chains each having not over two hydrophobic carbons connected together.
4. The combination of claim 1 in which the hydrophilic moiety weighs at least I percent more than the lipophilic moiety.
5. The combination of claim 1 in which the imidazoline surfactant is:
CH; CHzCIIzOCHZC 0 ON.
Cine 0 0 N3.
where R is a C to C alkyl, and the amine dipropionate surfactant is C H N(CH CH COONa) or '6. In the method of fighting a fire in a body of liquid hydrocarbon held in a container by introducing an aqueous foam into the body of liquid from a location below the surface of that body, the improvement according to which the aqueous foam is the foamed composition of claim 1.
7. In the method of fighting a fire in a body of liquid hydrocarbon held in a container by introducing an aqueous foam into the body of liquid from a location below the surface of that body, the improvement according to which the aqueous foam is the foamed composition of claim 4.

Claims (7)

1. IN AN AQUEOUS FILM-FORMING FIRE-FIGHTING FOAMABLE LIQUID CONTAING DISSOLVED FLUOROCARBON AND SILICONE SURFACTANTS IN AMOUNTS THAT GIVE THE LIQUID A SURFACE TENSION AT LEAST AS LOW AS 19 DYNES PER CENTIMETER BUT DO NOT GIVE IT GOOD FOAMABILITY AND ALSO CONTAINING ONE OR MORE FOAMABILITY-INCREASING SURFACTANTS THAT ARE NEITHER FLUOROCARBONS NOR SILICONES, TO BRING THE FOAMABILITY OF THE LIQUID UP TO THE LEVEL NEEDED FOR A FIRE-FIGHTING FOAM, THE IMPROVEMENT ACCORDING TO WHICH AT LEAST 40 PERCENT OF THE FOAMABILITY-INCREASING SURFACTANTS IS AN IMIDAZOLINE OR AMINE DI-PROPIONATE SURFACTANT WITH HYDROPHILIC AND LIPOPHILIC MOIETIES OF WHICH THE HYDROPHILIC MOIETY HAS AT LEAST THREE HYDROPHILE UNITS SELECTED FROM THE CLASS CONSISTING OF HYDROXYL, CARBOXYL, SULFO AND NITROGEN, AND WEIGHTS AT LEAST 80 PERCENT MORE THAN THE LIPOPHILIC MOIETY.
2. The combination of claim 1 in which the lipophilic moiety is in the form of a hydrocarbon chain not over 10 carbons long.
3. The combination of claim 1 in which the imidazoline has one of its ring nitrogens quaternized with two carboxylated carbon chains each having not over two hydrophobic carbons connected together.
4. The combination of claim 1 in which the hydrophilic moiety weighs at least 120 percent more than the lipophilic moiety.
5. The combination of claim 1 in which the imidazoline surfactant is:
6. In the method of fighting a fire in a body of liquid hydrocarbon held in a container by introducing an aqueous foam into the body of liquid from a location below the surface of that body, the improvement according to which the aqueous foam is the foamed composition of claim 1.
7. In the method of fighting a fire in a body of liquid hydrocarbon held in a container by introducing an aqueous foam into the body of liquid from a location below the surface of that body, the improvement according to which the aqueous foam is the foamed composition of claim 4.
US00254404A 1971-04-06 1972-05-18 Film-forming fire fighting composition Expired - Lifetime US3849315A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
US00254404A US3849315A (en) 1972-05-18 1972-05-18 Film-forming fire fighting composition
JP47086735A JPS5233920B2 (en) 1972-05-18 1972-08-31
AU55172/73A AU470208B2 (en) 1972-05-18 1973-05-03 Film-forming firefighting composition
GB2354873A GB1431982A (en) 1972-05-18 1973-05-17 Film-forming firefighting composition
CA171,787A CA994539A (en) 1972-05-18 1973-05-18 Film-forming fire fighting composition
US05/525,175 US4038195A (en) 1972-05-18 1974-11-19 Fire fighting compositions
US05/670,252 US4060489A (en) 1971-04-06 1976-03-25 Fire fighting with thixotropic foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US00254404A US3849315A (en) 1972-05-18 1972-05-18 Film-forming fire fighting composition

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US13176371A Continuation-In-Part 1971-04-06 1971-04-06

Related Child Applications (3)

Application Number Title Priority Date Filing Date
US30747972A Continuation-In-Part 1972-11-17 1972-11-17
US05/369,584 Continuation-In-Part US3957657A (en) 1971-04-06 1973-06-13 Fire fighting
US05/525,175 Continuation-In-Part US4038195A (en) 1972-05-18 1974-11-19 Fire fighting compositions

Publications (1)

Publication Number Publication Date
US3849315A true US3849315A (en) 1974-11-19

Family

ID=22964185

Family Applications (1)

Application Number Title Priority Date Filing Date
US00254404A Expired - Lifetime US3849315A (en) 1971-04-06 1972-05-18 Film-forming fire fighting composition

Country Status (5)

Country Link
US (1) US3849315A (en)
JP (1) JPS5233920B2 (en)
AU (1) AU470208B2 (en)
CA (1) CA994539A (en)
GB (1) GB1431982A (en)

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3957658A (en) * 1971-04-06 1976-05-18 Philadelphia Suburban Corporation Fire fighting
US4038195A (en) * 1972-05-18 1977-07-26 Philadelphia Suburban Corporation Fire fighting compositions
US4042522A (en) * 1975-03-24 1977-08-16 Ciba-Geigy Corporation Aqueous wetting and film forming compositions
US4060132A (en) * 1974-11-19 1977-11-29 Philadelphia Suburban Corporation Fire fighting with thixotropic foam
US4060489A (en) * 1971-04-06 1977-11-29 Philadelphia Suburban Corporation Fire fighting with thixotropic foam
US4149599A (en) * 1976-03-25 1979-04-17 Philadelphia Suburban Corporation Fighting fire
US4390069A (en) * 1979-10-01 1983-06-28 Grumman Aerospace Corporation Trifluorobromomethane foam fire fighting system
US4859349A (en) * 1987-10-09 1989-08-22 Ciba-Geigy Corporation Polysaccharide/perfluoroalkyl complexes
US5945025A (en) * 1997-12-08 1999-08-31 Cunningham; James A. Fire extinguishing composition and method for fire extinguishing
US6231778B1 (en) 1999-12-29 2001-05-15 Ansul Incorporated Aqueous foaming fire extinguishing composition
US6550750B1 (en) 1997-05-09 2003-04-22 David Kalkstein Apparatus for producing foamable compositions and other compositions
US20070085060A1 (en) * 2005-10-18 2007-04-19 Dario Santoro Method of making a fire extinguishing chemical
US20080146820A1 (en) * 2006-12-15 2008-06-19 Axel Hans-Joachim Herzog Phosphate fluorosurfactant and siloxane surfactant
EP1980611A2 (en) 2007-04-10 2008-10-15 Evonik Goldschmidt GmbH Use of anionic silicon tensides for creating foam
EP1980295A2 (en) 2007-04-10 2008-10-15 Evonik Goldschmidt GmbH Silicon tenside compounds and their use for producing foam
DE102008000845A1 (en) 2008-03-27 2009-10-01 Evonik Goldschmidt Gmbh Use of a composition containing silicon organic compounds and optionally surfactant active compounds with perfluorinated units, to produce fire-extinguishing foam, which is useful to clean device or apparatus, and reduce evaporation loss
DE102008054712A1 (en) 2008-12-16 2010-06-17 Evonik Goldschmidt Gmbh Use of amphoteric surfactants to produce foam
US7964552B2 (en) 2006-12-15 2011-06-21 E. I. Du Pont De Nemours And Company Fluorosurfactant with disproportionate effect
WO2012045080A1 (en) 2010-10-01 2012-04-05 Tyco Fire Products Lp Aqueous fire-fighting foams with reduced fluorine content
US8628682B2 (en) 2011-10-24 2014-01-14 E I Du Pont De Nemours And Company Compositions comprising a fluorosurfactant and a hydrotrope
WO2014144988A2 (en) 2013-03-15 2014-09-18 Tyco Fire Products Lp Perfluoroalkyl composition with reduced chain length
WO2014153140A1 (en) 2013-03-14 2014-09-25 Tyco Fire & Security Gmbh Trimethylglycine as a freeze suppressant in fire fighting foams
WO2016130810A1 (en) 2015-02-13 2016-08-18 Tyco Fire Products Lp Use of an indicator as a marker in foam concentrates
WO2017161156A1 (en) 2016-03-18 2017-09-21 Tyco Fire Products Lp Polyorganosiloxane compounds as active ingredients in fluorine free fire suppression foams
WO2017161162A1 (en) 2016-03-18 2017-09-21 Tyco Fire Products Lp Organosiloxane compounds as active ingredients in fluorine free fire suppression foams
WO2018022763A1 (en) 2016-07-29 2018-02-01 Tyco Fire Products Lp Firefighting foam compositions containing deep eutectic solvents
US10870030B2 (en) 2014-04-02 2020-12-22 Tyco Fire Products Lp Fire extinguishing compositions and method

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51108788A (en) * 1975-03-20 1976-09-27 Kogyo Gijutsuin
JPS51117589A (en) * 1975-04-09 1976-10-15 Agency Of Ind Science & Technol Glass sealed solar battery equipment and its manufacturing method
JPS5836251Y2 (en) * 1977-05-25 1983-08-16 ヤンマー農機株式会社 Reaping conveyance device in combine harvester
JP4678338B2 (en) * 2006-06-06 2011-04-27 信越化学工業株式会社 Organic resin flame retardant additive, flame retardant resin composition and molded product thereof
CN105854216B (en) * 2016-04-01 2019-02-05 中国民用航空飞行学院 Aqueous film-forming foam extinguishing agent based on short carbon fluorine chain
CN110935392B (en) * 2019-11-26 2022-02-15 沈阳建筑大学 Anti-freezing organic foaming liquid for foam-blocked environment-friendly toilet and preparation method thereof

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4060489A (en) * 1971-04-06 1977-11-29 Philadelphia Suburban Corporation Fire fighting with thixotropic foam
US3957658A (en) * 1971-04-06 1976-05-18 Philadelphia Suburban Corporation Fire fighting
US4038195A (en) * 1972-05-18 1977-07-26 Philadelphia Suburban Corporation Fire fighting compositions
US4060132A (en) * 1974-11-19 1977-11-29 Philadelphia Suburban Corporation Fire fighting with thixotropic foam
US4042522A (en) * 1975-03-24 1977-08-16 Ciba-Geigy Corporation Aqueous wetting and film forming compositions
US4149599A (en) * 1976-03-25 1979-04-17 Philadelphia Suburban Corporation Fighting fire
US4390069A (en) * 1979-10-01 1983-06-28 Grumman Aerospace Corporation Trifluorobromomethane foam fire fighting system
US4859349A (en) * 1987-10-09 1989-08-22 Ciba-Geigy Corporation Polysaccharide/perfluoroalkyl complexes
US6550750B1 (en) 1997-05-09 2003-04-22 David Kalkstein Apparatus for producing foamable compositions and other compositions
US5945025A (en) * 1997-12-08 1999-08-31 Cunningham; James A. Fire extinguishing composition and method for fire extinguishing
US6231778B1 (en) 1999-12-29 2001-05-15 Ansul Incorporated Aqueous foaming fire extinguishing composition
US20070085060A1 (en) * 2005-10-18 2007-04-19 Dario Santoro Method of making a fire extinguishing chemical
US20080146820A1 (en) * 2006-12-15 2008-06-19 Axel Hans-Joachim Herzog Phosphate fluorosurfactant and siloxane surfactant
US7964552B2 (en) 2006-12-15 2011-06-21 E. I. Du Pont De Nemours And Company Fluorosurfactant with disproportionate effect
EP1980611A2 (en) 2007-04-10 2008-10-15 Evonik Goldschmidt GmbH Use of anionic silicon tensides for creating foam
EP1980295A2 (en) 2007-04-10 2008-10-15 Evonik Goldschmidt GmbH Silicon tenside compounds and their use for producing foam
DE102007016966A1 (en) 2007-04-10 2008-10-16 Evonik Goldschmidt Gmbh Silicone surfactant compositions and their use for producing foam
DE102007016965A1 (en) 2007-04-10 2008-10-16 Evonik Goldschmidt Gmbh Use of anionic silicone surfactants to produce foam
DE102008000845A1 (en) 2008-03-27 2009-10-01 Evonik Goldschmidt Gmbh Use of a composition containing silicon organic compounds and optionally surfactant active compounds with perfluorinated units, to produce fire-extinguishing foam, which is useful to clean device or apparatus, and reduce evaporation loss
DE102008054712A1 (en) 2008-12-16 2010-06-17 Evonik Goldschmidt Gmbh Use of amphoteric surfactants to produce foam
EP2198932A2 (en) 2008-12-16 2010-06-23 Evonik Goldschmidt GmbH Use of amphoteric tensides for creating foam
WO2012045080A1 (en) 2010-10-01 2012-04-05 Tyco Fire Products Lp Aqueous fire-fighting foams with reduced fluorine content
US8628682B2 (en) 2011-10-24 2014-01-14 E I Du Pont De Nemours And Company Compositions comprising a fluorosurfactant and a hydrotrope
US10369395B2 (en) 2013-03-14 2019-08-06 Tyco Fire Products Lp Trimethylglycine as a freeze suppressant in fire fighting foams
WO2014153140A1 (en) 2013-03-14 2014-09-25 Tyco Fire & Security Gmbh Trimethylglycine as a freeze suppressant in fire fighting foams
WO2014144988A2 (en) 2013-03-15 2014-09-18 Tyco Fire Products Lp Perfluoroalkyl composition with reduced chain length
US10870030B2 (en) 2014-04-02 2020-12-22 Tyco Fire Products Lp Fire extinguishing compositions and method
US11305143B2 (en) 2014-04-02 2022-04-19 Tyco Fire Products Lp Fire extinguishing compositions and method
US11766582B2 (en) 2014-04-02 2023-09-26 Tyco Fire Products Lp Fire extinguishing compositions and method
US10786696B2 (en) 2015-02-13 2020-09-29 Tyco Fire Products Lp Use of an indicator as a marker in foam concentrates
WO2016130810A1 (en) 2015-02-13 2016-08-18 Tyco Fire Products Lp Use of an indicator as a marker in foam concentrates
WO2017161162A1 (en) 2016-03-18 2017-09-21 Tyco Fire Products Lp Organosiloxane compounds as active ingredients in fluorine free fire suppression foams
WO2017161156A1 (en) 2016-03-18 2017-09-21 Tyco Fire Products Lp Polyorganosiloxane compounds as active ingredients in fluorine free fire suppression foams
US10780305B2 (en) 2016-03-18 2020-09-22 Tyco Fire Products Lp Organosiloxane compounds as active ingredients in fluorine free fire suppression foams
US11173334B2 (en) 2016-03-18 2021-11-16 Tyco Fire Products Lp Polyorganosiloxane compounds as active ingredients in fluorine free fire suppression foams
WO2018022763A1 (en) 2016-07-29 2018-02-01 Tyco Fire Products Lp Firefighting foam compositions containing deep eutectic solvents
US11771938B2 (en) 2016-07-29 2023-10-03 Tyco Fire Products Lp Firefighting foam compositions containing deep eutectic solvents

Also Published As

Publication number Publication date
CA994539A (en) 1976-08-10
GB1431982A (en) 1976-04-14
JPS5233920B2 (en) 1977-08-31
AU470208B2 (en) 1976-03-04
AU5517273A (en) 1974-11-07
JPS4925796A (en) 1974-03-07

Similar Documents

Publication Publication Date Title
US3849315A (en) Film-forming fire fighting composition
US3957657A (en) Fire fighting
US3957658A (en) Fire fighting
US4060489A (en) Fire fighting with thixotropic foam
US4536298A (en) Aqueous foam fire extinguisher
US5434192A (en) High-stability foams for long-term suppression of hydrocarbon vapors
US3258423A (en) Method of extinguishing liquid hydrocarbon fires
AU634572B2 (en) Alcohol resistant aqueous film forming firefighting foam
US4149599A (en) Fighting fire
US4424133A (en) Fire-fighting compositions
US4060132A (en) Fire fighting with thixotropic foam
US4099574A (en) Fire-fighting compositions
US4387032A (en) Concentrates for fire-fighting foam
US4464267A (en) Preparing fire-fighting concentrates
US5391721A (en) Aqueous film forming foam concentrates for hydrophilic combustible liquids and method for modifying viscosity of same
US3661776A (en) Composition comprising a foam-forming fluoroaliphatic compound and a film-forming fluoroaliphatic compound
CN110507944B (en) High-concentration environment-friendly fluorine-free compressed air foam extinguishing agent
JPH06218075A (en) Water-based fire extinguishing agent
US4038195A (en) Fire fighting compositions
JP2001269421A (en) Fire-extinguishing chemical
CA1116386A (en) Fighting fire
US2748078A (en) Fire extinguishing foam-forming composition
WO1997028846A1 (en) Fire fighting foams utilising saponins
US3684018A (en) Foam-forming flame-extinguishing compositions containing alkylpolyalkoxysulfates, polyoxyethylene resin and symmetrical dibromotetrafluoroethane
US3578590A (en) Fire-extinguishing composition comprising ethoxylated alkylphenol and ethylene glycol mono lower alkyl ether

Legal Events

Date Code Title Description
AS Assignment

Owner name: ENTERRA CORPORATION; 150 GORDON DR., LIONVILLE, PA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:PHILADELPHIA SUBURBAN CORPORATION;REEL/FRAME:003985/0216

Effective date: 19820211

Owner name: ENTERRA CORPORATION, PENNSYLVANIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:PHILADELPHIA SUBURBAN CORPORATION;REEL/FRAME:003985/0216

Effective date: 19820211

AS Assignment

Owner name: NATIONAL FOAM SYSTEM, INC., LIONVILLE, PA A CORP.

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:ENTERRA CORPORATION;REEL/FRAME:004760/0317

Effective date: 19870610

Owner name: NATIONAL FOAM SYSTEM, INC.,PENNSYLVANIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ENTERRA CORPORATION;REEL/FRAME:004760/0317

Effective date: 19870610

AS Assignment

Owner name: CHUBB NATIONAL FOAM, INC.

Free format text: CHANGE OF NAME;ASSIGNOR:NATIONAL FOAM SYSTEM, INC.;REEL/FRAME:004996/0651

Effective date: 19880531

AS Assignment

Owner name: CHUBB NATIONAL FOAM, INC.

Free format text: CHANGE OF NAME;ASSIGNOR:NATIONAL FOAM SYSTEM, INC.;REEL/FRAME:005113/0652

Effective date: 19880502

STCF Information on status: patent grant

Free format text: PATENTED FILE - (OLD CASE ADDED FOR FILE TRACKING PURPOSES)

AS Assignment

Owner name: NATIONAL FOAM SYSTEM, INC., LIONVILLE, PA A PA COR

Free format text: RECORD TO DELETE PATENT NUMBERS ERRONEOUSLY LISTED ON;ASSIGNOR:ENTERRA CORPORATION;REEL/FRAME:005521/0463

Effective date: 19901003