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EP0621057B1 - Emulsifier for portable fire extinguishers - Google Patents

Emulsifier for portable fire extinguishers Download PDF

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Publication number
EP0621057B1
EP0621057B1 EP19940400801 EP94400801A EP0621057B1 EP 0621057 B1 EP0621057 B1 EP 0621057B1 EP 19940400801 EP19940400801 EP 19940400801 EP 94400801 A EP94400801 A EP 94400801A EP 0621057 B1 EP0621057 B1 EP 0621057B1
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EP
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Prior art keywords
fluorinated
emulsifier according
emulsifier
integer ranging
carbon atoms
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EP19940400801
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German (de)
French (fr)
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EP0621057A1 (en
Inventor
Gilbert Garcia
Elisabeth Morillon
Christian Varescon
Casimir Kalinka
Ivan Devaux
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EIDP Inc
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Elf Atochem SA
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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

Definitions

  • the present invention relates to the field of fire extinguishing and more particularly relates to foam concentrates for portable water spray extinguishers.
  • foaming base generally consists of a hydrolyzate of animal proteins (hair, horns, hooves, hemoglobin).
  • fluorosurfactants to obtain a fluoroprotein foam concentrate; such emulsifiers are described, for example, in patents GB 1,280,508, GB 1,368,463, US 4,424,133, EP 49,958, US 4,460,480, FR 2,230,384, GB 2,011,784 and WO 8803425.
  • the foaming base is composed of a mixture of hydrocarbon-based surfactants.
  • Film-forming fluorinated surfactants can also be incorporated.
  • AFFF foam concentrates the presence of the fluorinated surfactant makes it possible to produce a foam which, by decantation, forms an aqueous film floating above the surface of the hydrocarbon. The purpose of this aqueous film is not only to extinguish the fire, but also to prevent a possible re-ignition of the surface of the hydrocarbon.
  • Foam concentrates of this type have been described in numerous patents, in particular the following: GB 1 258 299, US 5 085 786, FR 2 347 426, US 3 957 657, FR 2 040 316, US 4 350 206, FR 3 562 156, FR 2 148 442, FR 2 407 724, FR 2 385 413, US 3 772 195, FR 2 397 847, US 3 661 776, US 3 839 425, FR 2 103 669, US 3 957 657, US 3 963,776 and FR 2,296,625.
  • the spreading coefficient must be positive, care must be taken that the interfacial tension ( ⁇ i ) is not too low in order to avoid emulsification of the hydrocarbon by the extinguishing composition or too great a thinning of the aqueous film.
  • the emulsification of the hydrocarbon by the extinguishing composition risks in fact causing the entrainment of part of the hydrocarbon inside the extinguishing foam, of contaminating the latter and of igniting it.
  • the thermal resistance of the aqueous film Another important factor vis-à-vis the re-ignition phenomenon is the thermal resistance of the aqueous film.
  • an excessive spreading speed leads to the formation of a very thin film which is not very resistant to heat; conversely, the films most resistant to heat are those with the slowest speed of formation. It is therefore important to find a compromise between the spreading speed and the thermal resistance of the aqueous film, this property being essential for obtaining good resistance to re-ignition.
  • the aqueous film which removes the hydrocarbon vapors can at any time, for example by stirring, be separated from the foam from which it comes and be found directly in contact with an ignited part. If its thermal resistance is too low, the film can be destroyed and release hydrocarbon vapors which ignite immediately and continue to destroy the rest of the film.
  • AFFF foam concentrates which are generally used with fire hoses are not suitable in a portable extinguisher designed to be carried and used by hand and which, in working order, has a mass less than or equal to 20 kg.
  • the amount of water available to dilute the foam concentrate to the use concentration (0.5 to 6%, most often 1 to 3%) is limited and generally set at 6 or 9 liters , while in the application system by means of a lance the quantity of water available is not limited. Therefore, to meet the certification standards for foaming liquids for hydrocarbon fires, an emulsifier for portable extinguisher must be much more efficient than a conventional emulsifier for fire hoses.
  • the portable extinguisher must extinguish with only 6 liters of foam concentrate solution diluted to 3% (French standard) S61-900), while in the case of extinction with a fire hose the maximum available quantity of foam concentrate solution diluted to 3% may be up to 28.5 liters (French standard S60-220) or 22 , 3 liters (UL 162 standard).
  • the non-fluorinated surfactant (d) can be chosen from the compounds of the following formulas: R 4 -OSO 3 M (IV-1) R 4 - (OC 2 H 4 ) r -OSO 3 M (IV-2) R 4 (OC 2 H 4 ) r -OH (IV-3) R 4 -CONH-C 2 H 4 -NH-C 2 H 4 OC 2 H 4 COOM '(IV-6) R 4 -NH-C 2 H 4 -COOH (IV-7) R 4 -N (C 2 H 4 COOM ') 2 (IV-8) R 4 -CONH-C 3 H 6 -N ⁇ (CH 3 ) 2 CH 2 COO ⁇ (IV-10) R 4 -N (CH 3 ) 2 ⁇ O in which R 4 represents an alkyl radical, linear or branched, containing from 8 to 18 carbon atoms, r is an integer ranging from 1 to 16, M denotes an alkali metal ion or
  • monoalkyl ethers there may be mentioned the monoethyl or monobutyl ether of ethylene glycol and the monobutyl ether of diethylene glycol, the latter being preferred.
  • the foam concentrates according to the invention can be prepared by simple mixing of the various constituents until homogenization. To accelerate homogenization, one can operate by heating to a temperature between room temperature and that of boiling of the mixture, preferably at a temperature between 30 and 60 ° C.
  • the pH of the foam concentrate is advantageously stabilized at a value at least equal to 7 (preferably between 8 and 10) by means of a weak base, for example ammonia or an organic base such as diethanolamine, triethanolamine, urea.
  • a weak base for example ammonia or an organic base such as diethanolamine, triethanolamine, urea.
  • the foam concentrates according to the invention can be used in a portable fire extinguisher in an amount of 0.5 to 6 parts by weight (preferably 1 to 3 parts) of foam concentrate per 100 parts by weight of water.
  • This test which indicates the speed of formation of the aqueous film on the surface of the hydrocarbon, is carried out by pouring 50 ml of hydrocarbon (heptane) into a Petri dish (diameter: 11.5 cm), the outer face of which is painted in black so that you can watch the film.
  • hydrocarbon heptane
  • Petri dish diameter: 11.5 cm
  • 0.1 ml of a 3% aqueous emulsifier solution is deposited using a micropipette.
  • the solution should be applied dropwise starting from the center and making an eccentric movement.
  • the stopwatch is started when the first drop is deposited and stopped when the film has covered the entire surface of the hydrocarbon. We note the time. If the total recovery is not obtained in less than a minute, the percentage of surface covered after one minute is noted.
  • the spreading is satisfactory if the total recovery is obtained in less than 30 seconds, preferably between 5 and 25 seconds.
  • the evaluation of the thermal resistance of the aqueous film is obtained by measuring the Limit Temperature of Film Stability (TLSF).
  • TLSF Limit Temperature of Film Stability
  • a good foam concentrate should lead to a TLSF higher than 35 ° C, preferably higher than around 40 ° C
  • the expansion is the ratio of the volume of foam produced from a 3% aqueous solution of foam concentrate to the initial volume.
  • 100 ml of 3% aqueous emulsifier solution is introduced into a 1 liter test tube, then the solution is beaten for one minute at the rate of one beat per second using a perforated circular piston (30 holes of 5 mm in diameter representing 25% of the surface) and fixed in its center to a metal rod.
  • a satisfactory foam concentrate must lead to an expansion at least equal to 8.
  • the surface tension ( ⁇ s ) with tap water and the interfacial tension ( ⁇ i ) with heptane are measured using a LAUDA tensiometer in accordance with ISO 304 and ISO 6889, but operating at 25 ° C .
  • B fluorinated amine oxide of formula: C 6 F 13 -CH 2 CH 2 -SO 2 NH-CH 2 CH 2 CH 2 -N (CH 3 ) 2 ⁇ 0 marketed by the Applicant in the form of a 40% hydroalcoholic solution.
  • C Alkyl (C 8 and C 10 ) -glucoside sold in the form of a 70% aqueous solution by the company UNION CARBIDE under the name Triton BG 10.
  • D3 Alkyl (C 12 and C 14 ) -amidopropylbetaine of formula: Alkyl-CONH-CH 2 CH 2 CH 2 -N ⁇ (CH 3 ) 2 CH 2 COO ⁇ sold in 30% aqueous solution under the name Ampho-tensid B4 by the company ZSCHIMMER and SCHWARTZ.
  • D4 Decyl ether sulfate of formula: C 10 H 21 (OC 2 H 4 ) 2 OSO 3 Na used in 30% aqueous solution.
  • E Mono-n.butyl ether of diethylene glycol: C 4 H 9 OC 2 H 4 -OC 2 H 4 OH
  • an emulsifier according to the invention is prepared, the active ingredient contents of which are as follows: Constituents Content (% ) AT 10.8 B 6.2 VS 3.3 D1 7.9 E 40.0 ethanol 5.4 water (qs 100%) 26.4
  • This composition brought to pH 9.3 by addition of diethanolamine, has the following characteristics: - freezing temperature -22 ⁇ 2 ° C - Volumic mass 1.065 - viscosity 18 mPa.s - refractive index 1,414 - ⁇ s (3% city water) 16.4 mN / m - ⁇ i (3% city water / heptane) 2.5 mN / m - flash point (in closed section) 50 ° C
  • this foam concentrate leads to the following performances: - spreading 20 seconds - TLSF 47 ° C - profusion 10.2 90 ml of this foam concentrate
  • the foam concentrates (b1) and (b2) prove to be less efficient than the foam concentrate of example 1-a.
  • Example 1-a is repeated, but the proportions of the various constituents are modified and / or the surfactant D1 is replaced by the compound D2.
  • Example 1-a The procedure is as in Example 1-a, but a part of the ether E is replaced by monoethylene glycol (hereinafter MEG) and the proportions of the various surfactants are varied.
  • MEG monoethylene glycol
  • Example 1-a The procedure is as in Example 1-a, but a part of the ether E is replaced by monoethylene glycol and at least one of the surfactants D2, D3 and D4 is used in place of D1 and / or instead of alkylglucoside C.

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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)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

Description

La présente invention concerne le domaine de l'extinction des incendies et a plus particulièrement pour objet des émulseurs pour extincteurs portatifs à eau pulvérisée.The present invention relates to the field of fire extinguishing and more particularly relates to foam concentrates for portable water spray extinguishers.

L'un des moyens bien connus pour éteindre des feux de liquides hydrocarbonés consiste à projeter sur le foyer une mousse obtenue en mélangeant sous pression élevée de l'eau et un émulseur à base d'agents tensio-actifs. La plupart des émulseurs disponibles sur le marché peuvent être rangés dans deux grandes catégories selon la nature de la base moussante. Dans une première famille d'émulseurs, la base moussante est généralement constituée d'un hydrolysat de protéines animales (poils, cornes, sabots, hémoglobine). A cette base protéinique peuvent être ajoutés des agents tensio-actifs fluorés pour obtenir un émulseur fluoroprotéinique; de tels émulseurs sont décrits, par exemple, dans les brevets GB 1 280 508, GB 1 368 463, US 4 424 133, EP 49958, US 4 460 480, FR 2 230 384, GB 2 011 784 et WO 8803425.One of the well-known means for extinguishing fires of hydrocarbon liquids consists in projecting onto the hearth a foam obtained by mixing water and an emulsifier based on surfactants under high pressure. Most foam concentrates available on the market can be divided into two main categories depending on the nature of the foaming base. In a first family of foam concentrates, the foaming base generally consists of a hydrolyzate of animal proteins (hair, horns, hooves, hemoglobin). To this protein base can be added fluorosurfactants to obtain a fluoroprotein foam concentrate; such emulsifiers are described, for example, in patents GB 1,280,508, GB 1,368,463, US 4,424,133, EP 49,958, US 4,460,480, FR 2,230,384, GB 2,011,784 and WO 8803425.

Dans l'autre grande famille d'émulseurs, la base moussante est composée d'un mélange d'agents tensio-actifs hydrocarbonés. Des agents tensio-actifs fluorés formant film peuvent également être incorporés. Dans ce dernier type d'émulseurs, connus dans le métier comme émulseurs AFFF, la présence du tensio-actif fluoré permet de produire une mousse qui par décantation forme un film aqueux flottant au-dessus de la surface de l'hydrocarbure. Ce film aqueux a pour but non seulement d'éteindre le feu, mais aussi d'empêcher une éventuelle réinflammation de la surface de l'hydrocarbure. Des émulseurs de ce type ont été décrits dans de nombreux brevets, en particulier les suivants: GB 1 258 299, US 5 085 786, FR 2 347 426, US 3 957 657, FR 2 040 316, US 4 350 206, FR 3 562 156, FR 2 148 442, FR 2 407 724, FR 2 385 413, US 3 772 195, FR 2 397 847, US 3 661 776, US 3 839 425, FR 2 103 669, US 3 957 657, US 3 963 776 et FR 2 296 625.In the other large family of foam concentrates, the foaming base is composed of a mixture of hydrocarbon-based surfactants. Film-forming fluorinated surfactants can also be incorporated. In this latter type of foam concentrate, known in the art as AFFF foam concentrates, the presence of the fluorinated surfactant makes it possible to produce a foam which, by decantation, forms an aqueous film floating above the surface of the hydrocarbon. The purpose of this aqueous film is not only to extinguish the fire, but also to prevent a possible re-ignition of the surface of the hydrocarbon. Foam concentrates of this type have been described in numerous patents, in particular the following: GB 1 258 299, US 5 085 786, FR 2 347 426, US 3 957 657, FR 2 040 316, US 4 350 206, FR 3 562 156, FR 2 148 442, FR 2 407 724, FR 2 385 413, US 3 772 195, FR 2 397 847, US 3 661 776, US 3 839 425, FR 2 103 669, US 3 957 657, US 3 963,776 and FR 2,296,625.

Afin d'obtenir une bonne résistance à la réinflammation, I'émulseur après dilution à l'eau et addition d'air doit produire une mousse formant, par décantation, un film aqueux qui s'étale sur toute la surface de l'hydrocarbure et dont la stabilité thermique soit la plus élevée possible. La condition d'équilibre thermodynamique nécessaire pour former le film aqueux est liée au coefficient d'étalement (CE) qui doit être positif. CE = γ HC - ( γ s + γ i)

Figure imgb0001

CE
= coefficient d'étalement en mN/m
γHC
= tension superficielle de l'hydrocarbure
γs
= tension superficielle de la composition extinctrice après dilution de l'émulseur
γi
= tension interfaciale entre l'hydrocarbure et la composition extinctrice après dilution de l'émulseur
In order to obtain good resistance to re-ignition, the foam concentrate after dilution with water and addition of air must produce a foam forming, by decantation, an aqueous film which spreads over the entire surface of the hydrocarbon and with the highest possible thermal stability. The condition of thermodynamic equilibrium necessary to form the aqueous film is linked to the spreading coefficient (CE) which must be positive. CE = γ HC - (( γ s + γ i)
Figure imgb0001
or
THIS
= spreading coefficient in mN / m
γ HC
= surface tension of the hydrocarbon
γ s
= surface tension of the extinguishing composition after dilution of the foam concentrate
γ i
= interfacial tension between the hydrocarbon and the extinguishing composition after dilution of the foam concentrate

Bien que le coefficient d'étalement doive être positif, il faut veiller à ce que la tension interfaciale (γi) ne soit pas trop faible afin d'éviter l'émulsification de l'hydrocarbure par la composition extinctrice ou un amincissement trop important du film aqueux. L'émulsification de l'hydrocarbure par la composition extinctrice risque en effet de provoquer l'entraînement d'une partie de l'hydrocarbure à l'intérieur de la mousse extinctrice, de contaminer celle-ci et de l'enflammer.Although the spreading coefficient must be positive, care must be taken that the interfacial tension (γ i ) is not too low in order to avoid emulsification of the hydrocarbon by the extinguishing composition or too great a thinning of the aqueous film. The emulsification of the hydrocarbon by the extinguishing composition risks in fact causing the entrainment of part of the hydrocarbon inside the extinguishing foam, of contaminating the latter and of igniting it.

Un autre facteur important vis-à-vis du phénomène de réinflammation est la résistance thermique du film aqueux. A cet égard, une vitesse d'étalement excessive conduit à la formation d'un film très mince et peu résistant à la chaleur; inversement, les films les plus résistants à la chaleur sont ceux dont la vitesse de formation est la plus lente. Il est donc important de trouver un compromis entre la vitesse d'étalement et la résistance thermique du film aqueux, cette propriété étant indispensable pour obtenir une bonne résistance à la réinflammation. En effet, le film aqueux qui supprime les vapeurs d'hydrocarbure peut à tout moment, par exemple par agitation, être séparé de la mousse dont il est issu et se retrouver directement en contact avec une partie enflammée. Si sa résistance thermique est trop faible, le film peut être détruit et libérer des vapeurs d'hydrocarbure qui s'enflamment aussitôt et continuent à détruire le reste du film.Another important factor vis-à-vis the re-ignition phenomenon is the thermal resistance of the aqueous film. In this respect, an excessive spreading speed leads to the formation of a very thin film which is not very resistant to heat; conversely, the films most resistant to heat are those with the slowest speed of formation. It is therefore important to find a compromise between the spreading speed and the thermal resistance of the aqueous film, this property being essential for obtaining good resistance to re-ignition. Indeed, the aqueous film which removes the hydrocarbon vapors can at any time, for example by stirring, be separated from the foam from which it comes and be found directly in contact with an ignited part. If its thermal resistance is too low, the film can be destroyed and release hydrocarbon vapors which ignite immediately and continue to destroy the rest of the film.

Les émulseurs AFFF qui sont généralement utilisés avec des lances à incendie ne conviennent pas dans un extincteur portatif conçu pour être porté et utilisé à la main et qui, en ordre de marche, a une masse inférieure ou égale à 20 kg. Dans un extincteur portatif, la quantité d'eau disponible pour diluer l'émulseur jusqu'à la concentration d'utilisation (0,5 à 6 %, le plus souvent 1 à 3 %) est limitée et fixée généralement à 6 ou 9 litres, alors que dans le système d'application au moyen d'une lance la quantité d'eau disponible n'est pas limitée. De ce fait, pour satisfaire aux normes d'homologation relatives aux liquides émulseurs pour feux d'hydrocarbures, un émulseur pour extincteur portatif doit être beaucoup plus performant qu'un émulseur classique pour lances à incendie. A titre d'exemple, pour obtenir la certification d'un extincteur de 6 litres pour des feux du type 144 B, l'extincteur portatif devra réaliser l'extinction avec seulement 6 litres de solution d'émulseur dilué à 3 % (norme française S61-900), alors que dans le cas de l'extinction avec une lance à incendie la quantité maximale disponible de solution d'émulseur dilué à 3 % pourra aller jusqu'à 28,5 litres (norme française S60-220) ou 22,3 litres (norme UL 162).AFFF foam concentrates which are generally used with fire hoses are not suitable in a portable extinguisher designed to be carried and used by hand and which, in working order, has a mass less than or equal to 20 kg. In a portable fire extinguisher, the amount of water available to dilute the foam concentrate to the use concentration (0.5 to 6%, most often 1 to 3%) is limited and generally set at 6 or 9 liters , while in the application system by means of a lance the quantity of water available is not limited. Therefore, to meet the certification standards for foaming liquids for hydrocarbon fires, an emulsifier for portable extinguisher must be much more efficient than a conventional emulsifier for fire hoses. For example, to obtain the certification of a 6 liter extinguisher for type 144 B fires, the portable extinguisher must extinguish with only 6 liters of foam concentrate solution diluted to 3% (French standard) S61-900), while in the case of extinction with a fire hose the maximum available quantity of foam concentrate solution diluted to 3% may be up to 28.5 liters (French standard S60-220) or 22 , 3 liters (UL 162 standard).

La présente invention a maintenant pour objet un émulseur pour extincteurs portatifs, caractérisé en ce qu'il consiste en une solution aqueuse contenant en poids:

  • (a) de 1 à 15 % (de préférence 2 à 12 %) d'au moins une bétaïne fluorée de formule générale :
    Figure imgb0002
  • (b) de 1 à 20 % (de préférence 3 à 15 %) d'au moins un oxyde d'amine fluorée de formule générale :
    Figure imgb0003
  • (c) de 2 à 8 % (de préférence 3 à 6 %) d'au moins un alkylglycoside de formule générale :

            H(C6H10O5)qOR3     (III)

  • (d) de 2 à 10 % (de préférence 3 à 8 %) d'au moins un agent tensio-actif non fluoré anionique, non-ionique ou amphotère autre que ceux de la formule III ;
  • (e) de 20 à 50 % (de préférence 30 à 45 %) d'au moins un monoalkyléther de mono- ou di-éthylène (ou propylène)glycol ;
   la teneur totale en composés fluorés a et b étant comprise entre 5 et 25 % (de préférence entre 7 et 18 %) et le rapport pondéral ( a + b )/( c + d
Figure imgb0004
) étant compris entre 1 et 2 (de préférence entre 1,3 et 1,7).The present invention now relates to an emulsifier for portable fire extinguishers, characterized in that it consists of an aqueous solution containing by weight:
  • (a) from 1 to 15% (preferably 2 to 12%) of at least one fluorinated betaine of general formula:
    Figure imgb0002
  • (b) from 1 to 20% (preferably 3 to 15%) of at least one fluorinated amine oxide of general formula:
    Figure imgb0003
  • (c) from 2 to 8% (preferably 3 to 6%) of at least one alkyl glycoside of general formula:

    H (C 6 H 10 O 5 ) q OR 3 (III)

  • (d) from 2 to 10% (preferably 3 to 8%) of at least one non-fluorinated anionic, nonionic or amphoteric surfactant other than those of formula III;
  • (e) from 20 to 50% (preferably 30 to 45%) of at least one monoalkyl ether of mono- or di-ethylene (or propylene) glycol;
the total content of fluorinated compounds a and b being between 5 and 25% (preferably between 7 and 18%) and the weight ratio ( a + b ) / ( c + d
Figure imgb0004
) being between 1 and 2 (preferably between 1.3 and 1.7).

Dans les formules I, II et III ci-dessus, les différents symboles ont les significations suivantes :

  • Rf et RF, identiques ou différents, représentent chacun un radical perfluoroalkyle, linéaire ou ramifié, contenant au moins 6 atomes de carbone, de préférence de 6 à 16 atomes de carbone ;
  • m et m', identiques ou différents, sont chacun un nombre entier allant de 0 à 6, de préférence égal à 0 ou 2,
  • X et X', identiques ou différents, désignent chacun un groupe CO ou SO2, de préférence un groupe SO2;
  • R et R', identiques ou différents, représentent chacun un atome d'hydrogène ou un radical méthyle ou éthyle ;
  • n et n', identiques ou différents, sont chacun un nombre entier allant de 1 à 5, de préférence égal à 3 ;
  • R1, R1', R2 et R2', identiques ou différents, représentent chacun un radical méthyle ou éthyle ;
  • p est un nombre entier allant de 1 à 5, de préférence égal à 1 ou 2 ;
  • Y désigne un groupement SO3 , OSO3 , ou COO ;
  • q est un nombre entier allant de 1 à 6, de préférence égal à 1 ou 2 ;
  • R3 représente un radical alkyle, linéaire ou ramifié, contenant de 6 à 18 atomes de carbone, de préférence 8 à 14 atomes de carbone.
In the formulas I, II and III above, the different symbols have the following meanings:
  • R f and R F , identical or different, each represent a perfluoroalkyl radical, linear or branched, containing at least 6 carbon atoms, preferably from 6 to 16 carbon atoms;
  • m and m ', identical or different, are each an integer ranging from 0 to 6, preferably equal to 0 or 2,
  • X and X ', identical or different, each denote a CO or SO 2 group , preferably an SO 2 group;
  • R and R ', identical or different, each represent a hydrogen atom or a methyl or ethyl radical;
  • n and n ', identical or different, are each an integer ranging from 1 to 5, preferably equal to 3;
  • R 1 , R 1 ' , R 2 and R 2' , identical or different, each represent a methyl or ethyl radical;
  • p is an integer ranging from 1 to 5, preferably equal to 1 or 2;
  • Y denotes a group SO 3 , OSO 3 , or COO ;
  • q is an integer ranging from 1 to 6, preferably equal to 1 or 2;
  • R 3 represents an alkyl radical, linear or branched, containing from 6 to 18 carbon atoms, preferably 8 to 14 carbon atoms.

A titre non limitatif, l'agent tensio-actif non fluoré (d) peut-être choisi parmi les composés de formules suivantes:

        R4-OSO3M     (IV-1)



        R4-(OC2H4)r-OSO3M     (IV-2)



        R4(OC2H4)r-OH     (IV-3)

Figure imgb0005


        R4-CONH-C2H4-NH-C2H4OC2H4COOM'     (IV-6)



        R4-NH-C2H4-COOH     (IV-7)



        R4-N(C2H4COOM')2     (IV-8)

Figure imgb0006


        R4-CONH-C3H6-N(CH3)2CH2COO     (IV-10)

R 4 -N(CH 3 ) 2 → O
Figure imgb0007
dans lesquelles R4 représente un radical alkyle, linéaire ou ramifié, contenant de 8 à 18 atomes de carbone, r est un nombre entier allant de 1 à 16, M désigne un ion métallique alcalin ou ammonium quaternaire et M' un ion métallique alcalin.By way of non-limiting example, the non-fluorinated surfactant (d) can be chosen from the compounds of the following formulas:

R 4 -OSO 3 M (IV-1)



R 4 - (OC 2 H 4 ) r -OSO 3 M (IV-2)



R 4 (OC 2 H 4 ) r -OH (IV-3)

Figure imgb0005


R 4 -CONH-C 2 H 4 -NH-C 2 H 4 OC 2 H 4 COOM '(IV-6)



R 4 -NH-C 2 H 4 -COOH (IV-7)



R 4 -N (C 2 H 4 COOM ') 2 (IV-8)

Figure imgb0006


R 4 -CONH-C 3 H 6 -N (CH 3 ) 2 CH 2 COO (IV-10)

R 4 -N (CH 3 ) 2 → O
Figure imgb0007
in which R 4 represents an alkyl radical, linear or branched, containing from 8 to 18 carbon atoms, r is an integer ranging from 1 to 16, M denotes an alkali metal ion or quaternary ammonium and M 'an alkali metal ion.

Comme exemples non limitatifs de monoalkyléthers (e), on peut citer l'éther monoéthylique ou monobutylique de l'éthylèneglycol et l'éther monobutylique du diéthylèneglycol, ce dernier étant préféré.As nonlimiting examples of monoalkyl ethers (e), there may be mentioned the monoethyl or monobutyl ether of ethylene glycol and the monobutyl ether of diethylene glycol, the latter being preferred.

Des émulseurs plus particulièrement préférés sont ceux qui contiennent:

  • comme constituants (a), un mélange de bétaïnes fluorées de formule :

            CxF2x+1-CH2CH2-SO2NH-CH2CH2CH2-N(CH3)2CH2COO

    dans laquelle x est un nombre entier pair allant de 6 à 16, la teneur du mélange en bétaïne à radical C6F13 étant d'au moins 50 % en poids;
  • comme constituant (b), l'oxyde d'amine fluorée de formule : C 6 F 13 CH 2 CH 2 -SO 2 NH-CH 2 CH 2 CH 2 -N(CH 3 ) 2 → O
    Figure imgb0008
  • comme constituant (d), un amido éther propionate de formule (IV-6), un alkyl β-iminodipropionate de formule (IV-8) ou une alkylamidopropylbétaïne de formule (IV-10).
More particularly preferred emulsifiers are those which contain:
  • as constituents (a), a mixture of fluorinated betaines of formula:

    C x F 2x + 1 -CH 2 CH 2 -SO 2 NH-CH 2 CH 2 CH 2 -N (CH 3 ) 2 CH 2 COO

    in which x is an even whole number ranging from 6 to 16, the content of the mixture of betaine with a C 6 F 13 radical being at least 50% by weight;
  • as constituent (b), the fluorinated amine oxide of formula: VS 6 F 13 CH 2 CH 2 -SO 2 NH-CH 2 CH 2 CH 2 -N (CH 3 ) 2 → O
    Figure imgb0008
  • as constituent (d), an amido ether propionate of formula (IV-6), an alkyl β-iminodipropionate of formula (IV-8) or an alkylamidopropyl betaine of formula (IV-10).

Les émulseurs selon l'invention peuvent être préparés par simple mélange des différents constituants jusqu'à homogénéisation. Pour accélérer l'homogénéisation, on peut opérer en chauffant à une température comprise entre la température ambiante et celle d'ébullition du mélange, de préférence à une température comprise entre 30 et 60°C.The foam concentrates according to the invention can be prepared by simple mixing of the various constituents until homogenization. To accelerate homogenization, one can operate by heating to a temperature between room temperature and that of boiling of the mixture, preferably at a temperature between 30 and 60 ° C.

Le pH de l'émulseur est avantageusement stabilisé à une valeur au moins égale à 7 (de préférence entre 8 et 10) au moyen d'une base faible, par exemple l'ammoniaque ou une base organique telle que la diéthanolamine, la triéthanolamine, l'urée.The pH of the foam concentrate is advantageously stabilized at a value at least equal to 7 (preferably between 8 and 10) by means of a weak base, for example ammonia or an organic base such as diethanolamine, triethanolamine, urea.

Si on le désire, on peut éventuellement incorporer aux émulseurs selon l'invention divers additifs tels que:

  • un agent antigel comme l'éthylèneglycol ou le propyléneglycol,
  • un co-solvant, par exemple un alcool inférieur (C1 à C4),
  • un anticorrosif tel que le tolyltriazole ou le nitrite de sodium,
  • un conservateur tel que le benzoate de sodium, le fomaldéhyde, l'o-phénylphénol ou le dichlorophène.
If desired, various additives such as:
  • an antifreeze agent such as ethylene glycol or propylene glycol,
  • a co-solvent, for example a lower alcohol (C1 to C4),
  • an anticorrosive such as tolyltriazole or sodium nitrite,
  • a preservative such as sodium benzoate, fomaldehyde, o-phenylphenol or dichlorophene.

Les émulseurs selon l'invention peuvent être utilisés dans un extincteur portatif à raison de 0,5 à 6 parties en poids (de préférence 1 à 3 parties) d'émulseur pour 100 parties en poids d'eau.The foam concentrates according to the invention can be used in a portable fire extinguisher in an amount of 0.5 to 6 parts by weight (preferably 1 to 3 parts) of foam concentrate per 100 parts by weight of water.

Les performances des émulseurs selon l'invention peuvent être évaluées par les test suivantsThe performance of the foam concentrates according to the invention can be evaluated by the following tests

Test d'étalementSpreading test

Ce test qui indique la vitesse de formation du film aqueux sur la surface de l'hydrocarbure est réalisé en versant 50 ml d'hydrocarbure (heptane) dans une boite de Petri (diamètre: 11,5 cm) dont la face extérieure est peinte en noir afin de pouvoir observer le film. Lorsque la surface est immobile, on dépose à l'aide d'une micropipette 0,1 ml d'une solution aqueuse à 3 % d'émulseur. La solution doit être déposée goutte à goutte en partant du centre et en effectuant un mouvement excentrique. Le chronomètre est déclenché au moment du dépôt de la première goutte et arrêté lorsque le film a recouvert toute la surface de l'hydrocarbure. On note le temps. Si le recouvrement total n'est pas obtenu en moins d'une minute, on note le pourcentage de surface recouverte après une minute.This test, which indicates the speed of formation of the aqueous film on the surface of the hydrocarbon, is carried out by pouring 50 ml of hydrocarbon (heptane) into a Petri dish (diameter: 11.5 cm), the outer face of which is painted in black so that you can watch the film. When the surface is stationary, 0.1 ml of a 3% aqueous emulsifier solution is deposited using a micropipette. The solution should be applied dropwise starting from the center and making an eccentric movement. The stopwatch is started when the first drop is deposited and stopped when the film has covered the entire surface of the hydrocarbon. We note the time. If the total recovery is not obtained in less than a minute, the percentage of surface covered after one minute is noted.

L'étalement est satisfaisant si le recouvrement total est obtenu en moins de 30 secondes, de préférence entre 5 et 25 secondes.The spreading is satisfactory if the total recovery is obtained in less than 30 seconds, preferably between 5 and 25 seconds.

Test de résistance thermiqueThermal resistance test

L'évaluation de la résistance thermique du film aqueux est obtenue en mesurant la Température Limite de Stabilité du Film (TLSF). Ce test qui ne peut être effectué que dans le cas où la totalité de la surface de l'hydrocarbure est recouverte par le film est réalisé dans un récipient de mesure en laiton d'un diamètre de 6,5 cm et d'un volume total de 100 ml, placé sur une plaque chauffante thermostatée. Dans ce récipient, on verse 80 ml d'hydrocarbure (heptane) et, lorsque la surface est immobile, on y dépose 0,1 ml d'une solution aqueuse à 3 % d'émulseur comme indiqué pour le test d'étalement. Après 60 secondes, on place l'extrémité d'un thermomètre au contact du film aqueux et une flamme à environ 1 cm au-dessus du film. Le thermostat est réglé pour une augmentation de température de 4°C/min. On note la température (TLSF) à laquelle se produit l'inflammation de l'hydrocarbure.The evaluation of the thermal resistance of the aqueous film is obtained by measuring the Limit Temperature of Film Stability (TLSF). This test, which can only be carried out if the entire surface of the hydrocarbon is covered by the film, is carried out in a brass measuring container with a diameter of 6.5 cm and a total volume. 100 ml, placed on a thermostated heating plate. In this container, 80 ml of hydrocarbon (heptane) are poured and, when the surface is stationary, 0.1 ml of an aqueous solution of 3% foam concentrate is deposited therein as indicated for the spreading test. After 60 seconds, the end of a thermometer is placed in contact with the aqueous film and a flame about 1 cm above the film. The thermostat is set for a temperature increase of 4 ° C / min. The temperature (TLSF) at which the ignition of the hydrocarbon occurs is noted.

Un bon émulseur doit conduire à une TLSF supérieure à 35°C, de préférence supérieure à environ 40°CA good foam concentrate should lead to a TLSF higher than 35 ° C, preferably higher than around 40 ° C

FoisonnementSpreading

Le foisonnement (ou taux d'expansion) est le rapport du volume de mousse produit à partir d'une solution aqueuse à 3 % d'émulseur au volume initial. Pour déterminer le foisonnement, on introduit dans une éprouvette de 1 litre 100 ml de solution aqueuse à 3 % d'émulseur, puis la solution est battue pendant une minute au rythme de un battement par seconde à l'aide d'un piston circulaire perforé (30 trous de 5 mm de diamètre représentant 25 % de la surface) et fixé en son centre à une tige métallique.The expansion (or expansion rate) is the ratio of the volume of foam produced from a 3% aqueous solution of foam concentrate to the initial volume. To determine the overrun, 100 ml of 3% aqueous emulsifier solution is introduced into a 1 liter test tube, then the solution is beaten for one minute at the rate of one beat per second using a perforated circular piston (30 holes of 5 mm in diameter representing 25% of the surface) and fixed in its center to a metal rod.

Un émulseur satisfaisant doit conduire à un foisonnement au moins égal à 8.A satisfactory foam concentrate must lead to an expansion at least equal to 8.

Tensions superficielle et interfacialeSurface and interfacial tensions

La tension superficielle (γs) avec l'eau de ville et la tension interfaciale (γi) avec l'heptane sont mesurées au moyen d'un tensiomètre LAUDA conformément aux normes ISO 304 et ISO 6889, mais en opérant à 25°C.The surface tension (γ s ) with tap water and the interfacial tension (γ i ) with heptane are measured using a LAUDA tensiometer in accordance with ISO 304 and ISO 6889, but operating at 25 ° C .

Dans les exemples suivants qui illustrent l'invention sans la limiter, les pourcentages indiqués sont exprimés en poids et les principaux constituants utilisés sont désignés, pour simplifier, par les abréviations suivantes:
A = Mélange de bétaïnes fluorées de formule :

        CxF2x+1CH2CH2-SO2NH-CH2CH2CH2-N(CH3)2CH2COO

ayant la composition pondérale suivante: x % 6 70 8 23 10 5 12 1,5 14 0,4 16 0,1    utilisé sous forme de solution aqueuse à 45 %.
B = Oxyde d'amine fluorée de formule :

        C6F13-CH2CH2-SO2NH-CH2CH2CH2-N(CH3)2 → 0

commercialisé par la Demanderesse sous forme de solution hydroalcoolique à 40 %.
C = Alkyl (C8 et C10)-glucoside commercialisé sous forme de solution aqueuse à 70 % par la Société UNION CARBIDE sous la dénomination Triton BG 10.
D1 = Alkyl (C8 et C10) amidoéther propionate de formule :

        Alkyl-CONH-CH2CH2-NH-CH2CH2-OCH2CH2COONa

commercialisé sous forme de solution aqueuse à 50 % par la Société REWO sous la dénomination Rewoteric AMVSF
D2 = N-lauryl-β-iminodipropionate de formule :

Figure imgb0009
commercialisé en solution aqueuse à 30 % par la Société HENKEL sous la dénomination Deriphat 160C.
D3 = Alkyl (C12 et C14)-amidopropylbétaïne de formule :

        Alkyl-CONH-CH2CH2CH2-N(CH3)2CH2COO

commercialisé en solution aqueuse à 30 % sous la dénomination Ampho-tensid B4 par la Société ZSCHIMMER et SCHWARTZ.
D4 = Décyl éther sulfate de formule :

        C10H21(OC2H4)2OSO3Na

utilisé en solution aqueuse à 30 %.
E = Mono-n.butyléther du diéthylèneglycol:

        C4H9O-C2H4-O-C2H4OH

In the following examples which illustrate the invention without limiting it, the percentages indicated are expressed by weight and the main constituents used are designated, for simplicity, by the following abbreviations:
A = Mixture of fluorinated betaines of formula:

C x F 2x + 1 CH 2 CH 2 -SO 2 NH-CH 2 CH 2 CH 2 -N (CH 3 ) 2 CH 2 COO

having the following weight composition: x % 6 70 8 23 10 5 12 1.5 14 0.4 16 0.1 used in the form of a 45% aqueous solution.
B = fluorinated amine oxide of formula:

C 6 F 13 -CH 2 CH 2 -SO 2 NH-CH 2 CH 2 CH 2 -N (CH 3 ) 2 → 0

marketed by the Applicant in the form of a 40% hydroalcoholic solution.
C = Alkyl (C 8 and C 10 ) -glucoside sold in the form of a 70% aqueous solution by the company UNION CARBIDE under the name Triton BG 10.
D1 = Alkyl (C 8 and C 10 ) amidoether propionate of formula:

Alkyl-CONH-CH 2 CH 2 -NH-CH 2 CH 2 -OCH 2 CH 2 COONa

marketed in the form of a 50% aqueous solution by the REWO Company under the name Rewoteric AMVSF
D2 = N-lauryl-β-iminodipropionate of formula:
Figure imgb0009
marketed in 30% aqueous solution by HENKEL under the name Deriphat 160C.
D3 = Alkyl (C 12 and C 14 ) -amidopropylbetaine of formula:

Alkyl-CONH-CH 2 CH 2 CH 2 -N (CH 3 ) 2 CH 2 COO

sold in 30% aqueous solution under the name Ampho-tensid B4 by the company ZSCHIMMER and SCHWARTZ.
D4 = Decyl ether sulfate of formula:

C 10 H 21 (OC 2 H 4 ) 2 OSO 3 Na

used in 30% aqueous solution.
E = Mono-n.butyl ether of diethylene glycol:

C 4 H 9 OC 2 H 4 -OC 2 H 4 OH

EXEMPLE 1EXAMPLE 1


a) En mélangeant à 40°C sous agitation modérée les quantités adéquates des produits commerciaux précités, on prépare un émulseur selon l'invention dont les teneurs en matières actives sont les suivantes: Constituants Teneurs (%) A 10,8 B 6,2 C 3,3 D1 7,9 E 40,0 éthanol 5,4 eau (qsp 100 %) 26,4
Cette composition, portée à pH 9,3 par addition de diéthanolamine, présente les caractéristiques suivantes: - température de congélation -22 ± 2°C - masse volumique 1,065 - viscosité 18 mPa.s - indice de réfraction 1,414 - γs (3 % eau de ville) 16,4 mN/m - γi (3 % eau de ville/heptane) 2,5 mN/m - point éclair (en coupe fermée) 50 °C
Soumis aux tests décrits précédemment, cet émulseur conduit aux performances suivantes: - étalement 20 secondes - TLSF 47°C - foisonnement 10,2
On place 90 ml de cet émulseur dans la cartouche d'un extincteur portatif de 6 litres, puis on teste son efficacité sur foyer d'heptane 144 B (norme NF S61-900). L'extinction a été obtenue avec un excellent comportement face au phénomène de réinflammation. En effet, si après l'extinction on rompt le film aqueux flottant et enflamme les vapeurs d'hydrocarbure mises au contact de l'air, le film se reforme aussitôt et recouvre à nouveau totalement la surface de l'hydrocarbure, éteignant ainsi le foyer naissant.
b) A titre comparatif, on a préparé deux émulseurs (b1) et (b2) non conformes à la présente invention et amené leur pH à 8,5 au moyen de diéthanolamine. Leur composition et leurs performances sont résumées dans le tableau suivant: EMULSEUR b1 b2 Constituants (%) A 4,2 17,0 B 2,4 - C 6,5 3,3 D1 15,1 7,9 E 40,0 40,0 éthanol 6,0 3,0 eau 25,8 28,8 Performances : étalement (s) 15 60 TLSF (°C) 27 25 foisonnement 10 9,3

a) By mixing the appropriate quantities of the abovementioned commercial products at 40 ° C. with moderate stirring, an emulsifier according to the invention is prepared, the active ingredient contents of which are as follows: Constituents Content (% ) AT 10.8 B 6.2 VS 3.3 D1 7.9 E 40.0 ethanol 5.4 water (qs 100%) 26.4
This composition, brought to pH 9.3 by addition of diethanolamine, has the following characteristics: - freezing temperature -22 ± 2 ° C - Volumic mass 1.065 - viscosity 18 mPa.s - refractive index 1,414 - γ s (3% city water) 16.4 mN / m - γ i (3% city water / heptane) 2.5 mN / m - flash point (in closed section) 50 ° C
Subjected to the tests described above, this foam concentrate leads to the following performances: - spreading 20 seconds - TLSF 47 ° C - profusion 10.2
90 ml of this foam concentrate are placed in the cartridge of a 6 liter portable fire extinguisher, then its effectiveness is tested on a heptane 144 B hearth (standard NF S61-900). The extinction was obtained with excellent behavior in the face of the phenomenon of re-ignition. In fact, if after the extinction the floating aqueous film is broken and ignites the hydrocarbon vapors brought into contact with the air, the film is reformed immediately and completely covers the surface of the hydrocarbon again, thus extinguishing the hearth nascent.
b) By way of comparison, two emulsifiers (b1) and (b2) not in accordance with the present invention were prepared and brought their pH to 8.5 by means of diethanolamine. Their composition and performance are summarized in the following table: EMULSEUR b1 b2 Constituents (%) AT 4.2 17.0 B 2.4 - VS 6.5 3.3 D1 15.1 7.9 E 40.0 40.0 ethanol 6.0 3.0 water 25.8 28.8 Performances : spread (s) 15 60 TLSF (° C) 27 25 profusion 10 9.3

Dans le test de résistance thermique (TLSF), les émulseurs (b1) et (b2) s'avèrent moins performants que l'émulseur de l'exemple 1-a.In the thermal resistance test (TLSF), the foam concentrates (b1) and (b2) prove to be less efficient than the foam concentrate of example 1-a.

EXEMPLE 2EXAMPLE 2

On répète l'exemple 1-a, mais on modifie les proportions des différents constituants et/ou on remplace l'agent tensio-actif D1 par le composé D2.Example 1-a is repeated, but the proportions of the various constituents are modified and / or the surfactant D1 is replaced by the compound D2.

Le tableau suivant indique la composition et les performances de trois émulseurs ainsi obtenus. EMULSEUR 2a 2b 2c Constituants (%) A 2,5 2,5 10,8 B 14,4 14,4 6,15 C 5,6 5,6 3,25 D1 5,5 - - D2 - 5,5 7,9 E 40 40 40 éthanol 12,6 12,6 5,4 eau 19,4 19,4 26,5 Performances : étalement (s) 7 6 10 TLSF (°C) 50 43 40 foisonnement 9,4 10,6 11 The following table indicates the composition and the performances of three foam concentrates thus obtained. EMULSEUR 2a 2b 2c Constituents (%) AT 2.5 2.5 10.8 B 14.4 14.4 6.15 VS 5.6 5.6 3.25 D1 5.5 - - D2 - 5.5 7.9 E 40 40 40 ethanol 12.6 12.6 5.4 water 19.4 19.4 26.5 Performances : spread (s) 7 6 10 TLSF (° C) 50 43 40 profusion 9.4 10.6 11

EXEMPLE 3EXAMPLE 3

On opère comme à l'exemple 1-a, mais on remplace une partie de l'éther E par du monoéthylèneglycol (ci-après MEG) et on fait varier les proportions des différents agents tensio-actifs.The procedure is as in Example 1-a, but a part of the ether E is replaced by monoethylene glycol (hereinafter MEG) and the proportions of the various surfactants are varied.

On prépare ainsi quatre émulseurs qu'on amène à pH 8,5 par addition de diéthanolamine. Leur composition et leurs performances sont rassemblées dans le tableau suivant. EMULSEUR 3a 3b 3c 3d Constituants (%) A 1,2 1,5 2,7 4,1 B 7 8,8 5,4 4,1 C 3,4 3,4 3,4 3,4 D2 3,4 3,4 3,4 3,4 E 30 30 30 30 MEG 15 15 15 15 éthanol 6,85 8,6 6,3 6 eau 33,15 29,3 33,8 34 Performances : étalement (s) 5 7 8 16 TLSF (°C) 41 43 42 40 foisonnement 10 9,2 9 9,2 Four emulsifiers are thus prepared which are brought to pH 8.5 by addition of diethanolamine. Their composition and performances are collated in the following table. EMULSEUR 3a 3b 3c 3d Constituents (%) AT 1.2 1.5 2.7 4.1 B 7 8.8 5.4 4.1 VS 3.4 3.4 3.4 3.4 D2 3.4 3.4 3.4 3.4 E 30 30 30 30 MEG 15 15 15 15 ethanol 6.85 8.6 6.3 6 water 33.15 29.3 33.8 34 Performances : spread (s) 5 7 8 16 TLSF (° C) 41 43 42 40 profusion 10 9.2 9 9.2

EXEMPLE 4EXAMPLE 4

On opère comme à l'exemple 1-a, mais on remplace une partie de l'éther E par du monoéthylèneglycol et on utilise au moins un des agents tensio-actifs D2, D3 et D4 à la place de D1 et/ou à la place de l'alkylglucoside C.The procedure is as in Example 1-a, but a part of the ether E is replaced by monoethylene glycol and at least one of the surfactants D2, D3 and D4 is used in place of D1 and / or instead of alkylglucoside C.

On prépare ainsi dix émulseurs différents:

  • 5 émulseurs selon l'invention (4a, 4b, 4c, 4d et 4e)
  • 5 émulseurs non conformes (4f, 4g, 4h, 4i et 4j)
qu'on porte à pH 8,5 au moyen de diéthanolamine avant d'effectuer les tests.Ten different foam concentrates are thus prepared:
  • 5 foam concentrates according to the invention (4a, 4b, 4c, 4d and 4e)
  • 5 non-compliant foam concentrates (4f, 4g, 4h, 4i and 4d)
which is brought to pH 8.5 by means of diethanolamine before carrying out the tests.

La composition et les performances de ces différents émulseurs sont réunies dans le tableau suivant: EMULSEUR 4a 4b 4c 4d 4e 4f 4g 4h 4i 4j Constituants (%) A 6,7 6,7 6,7 6,7 6,7 6,7 6,7 6,7 6,7 6,7 B 3,8 3,8 3,8 3,8 3,8 3,8 3,8 3,8 3,8 3,8 C 2,7 2,7 3,4 2,05 3,4 6,8 - - - - D2 4,1 - 1,7 4,75 3,4 - 3,4 - 6,8 - D3 - 2,7 - - - - 3,4 3,4 - 6,8 D4 - 1,4 1,7 - - - - 3,4 - - E 30 30 30 30 30 30 30 30 30 30 MEG 10 10 10 10 10 10 10 10 10 10 éthanol 7,3 7,3 7,3 7,3 7,3 7,3 7,3 7,3 7,3 7,3 eau 35,4 35,4 35,4 35,4 35,4 35,4 35,4 35,4 35,4 35,4 Performances : étalement (s) 18 15 12 14 15 15 * 20 ** * TLSF (°C) 39 37 37 37 40 44 - 29 - - foisonnement 10 9,6 10 11,3 10 7,3 10,3 9,5 10 8,8 * Moins de 10 % de la surface recouverte après 1 minute ** 30% de la surface recouverte après 1 minute The composition and performance of these different foam concentrates are gathered in the following table: EMULSEUR 4a 4b 4c 4d 4th 4f 4g 4h 4i 4d Constituents (%) AT 6.7 6.7 6.7 6.7 6.7 6.7 6.7 6.7 6.7 6.7 B 3.8 3.8 3.8 3.8 3.8 3.8 3.8 3.8 3.8 3.8 VS 2.7 2.7 3.4 2.05 3.4 6.8 - - - - D2 4.1 - 1.7 4.75 3.4 - 3.4 - 6.8 - D3 - 2.7 - - - - 3.4 3.4 - 6.8 D4 - 1.4 1.7 - - - - 3.4 - - E 30 30 30 30 30 30 30 30 30 30 MEG 10 10 10 10 10 10 10 10 10 10 ethanol 7.3 7.3 7.3 7.3 7.3 7.3 7.3 7.3 7.3 7.3 water 35.4 35.4 35.4 35.4 35.4 35.4 35.4 35.4 35.4 35.4 Performances : spread (s) 18 15 12 14 15 15 * 20 ** * TLSF (° C) 39 37 37 37 40 44 - 29 - - profusion 10 9.6 10 11.3 10 7.3 10.3 9.5 10 8.8 * Less than 10% of the surface covered after 1 minute ** 30% of the surface covered after 1 minute

L'examen des résultats montre qu'en l'absence d'alkylglucoside (émulseurs 4g, 4h, 4i et 4j) on n'obtient pas un étalement satisfaisant et/ou une TLSF élevée, mais que ce co-tensio-actif hydrocarboné seul (émulseur 4f) conduit à un foisonnement insuffisant.Examination of the results shows that in the absence of alkylglucoside (4g, 4h, 4i and 4d emulsifiers) a satisfactory spreading and / or a high TLSF is not obtained, but that this hydrocarbon cosurfactant alone (foam concentrate 4f) leads to insufficient expansion.

Claims (12)

  1. Emulsifier for portable fire extinguishers, characterized in that it consists of an aqueous solution containing by weight:
    (a) from 1 to 15% of at least one fluorinated betaine of general formula:
    Figure imgb0018
    in which Rf represents a linear or branched perfluoroalkyl radical containing at least 6 carbon atoms, m is an integer ranging from 0 to 6, X represents a group CO or SO2, R represents a hydrogen atom or a methyl or ethyl radical, n is an integer ranging from 1 to 5, R1 and R2, which may be identical or different, each represent a methyl or ethyl radical, p is an integer ranging from 1 to 5 and Y represents a group SO3 , OSO3 or COO;
    (b) from 1 to 20% of at least one fluorinated amine oxide of general formula:
    Figure imgb0019
    in which the symbols RF, m', n', X', R', R1' and R2' respectively have the same general meanings as Rf, m, n, X, R, R1 and R2;
    (c) from 2 to 8% of at least one alkyl glucoside of general formula:

            H(C6H10O5)qOR3     (III)

    in which q is an integer ranging from 1 to 6 and R3 represents a linear or branched alkyl radical containing from 6 to 18 carbon atoms;
    (d) from 2 to 10% of at least one anionic, nonionic or amphoteric non-fluorinated surface-active agent other than those of formula III;
    (e) from 20 to 50% of at least one monoalkyl ether of mono- or diethylene (or propylene) glycol;
       the total content of fluorinated compounds a and b being between 5 and 25% and the weight ratio ( a + b)/(c + d
    Figure imgb0020
    ) being between 1 and 2.
  2. Emulsifier according to Claim 1, characterized in that it contains from 2 to 12% of fluorinated betaine(s), 3 to 15% of fluorinated amine oxide(s), 3 to 6% of alkyl glucoside(s), 3 to 8% of surface-active agent(s) other than those of formula III, and 30 to 45% of monoalkyl ether(s) of mono- or diethylene (or propylene) glycol.
  3. Emulsifier according to Claim 1 or 2, in which the total content of fluorinated compounds is between 7 and 18%.
  4. Emulsifier according to one of Claims 1 to 3, in which the weight ratio ( a + b)/(c + d
    Figure imgb0021
    ) is between 1.3 and 1.7.
  5. Emulsifier according to one of Claims 1 to 4, in which the radicals Rf and/or RF contain from 6 to 16 carbon atoms, m and/or m' is equal to 0 or 2, n and/or n' is equal to 3, p is equal to 1 or 2, q is equal to 1 or 2, and the radical R3 contains from 8 to 14 carbon atoms.
  6. Emulsifier according to Claim 5, containing a mixture of fluorinated betaines of formula:

            CxF2x+1CH2CH2-SO2NH-CH2CH2CH2-N(CH3)2CH2COO

    in which x is an even integer ranging from 6 to 16, the C6F13 radical betaine content of the mixture being at least 50% by weight.
  7. Emulsifier according to Claim 5 or 6, in which the amine oxide is the compound . C 6 F 13 -CH 2 CH 2 -SO 2 NH-CH 2 CH 2 CH 2 -N(CH 3 ) 2 →0.
    Figure imgb0022
  8. Emulsifier according to one of Claims 1 to 7, in which the non-fluorinated surface-active agent (d) is chosen from the compounds of formulae:

            R4-OSO3M     (IV-1)



            R4-(OC2H4)r-OSO3M     (IV-2)



            R4(OC2H4)r-OH     (IV-3)

    Figure imgb0023


            R4-CONH-C2H4-NH-C2H4OC2H4COOM'     (IV-6)



            R4-NH-C2H4-COOH     (IV-7)



            R4-N(C2H4COOM')2     (IV-8)

    Figure imgb0024


            R4-CONH-C3H6-N(CH3)2CH2COO     (IV-10)

    R 4 -N(CH 3 ) 2 → O
    Figure imgb0025
    in which R4 represents a linear or branched alkyl radical containing from 8 to 18 carbon atoms, r is an integer ranging from 1 to 16, M denotes an alkali metal ion or a quaternary ammonium ion and M' an alkali metal ion.
  9. Emulsifier according to one of Claims 1 to 8, in which the ether (e) is diethylene glycol monobutyl ether.
  10. Emulsifier according to one of Claims 1 to 9, stabilized at a pH at least equal to 7, preferably between 8 and 10.
  11. Emulsifier according to one of Claims 1 to 10, additionally comprising an alcoholic co-solvent, an antifreeze, a preservative and/or an anti-corrosion agent.
  12. Use of an emulsifier according to one of Claims 1 to 11 in a portable extinguisher, in a proportion of 0.5 to 6 parts by weight, preferably 1 to 3 parts, of emulsifier per 100 parts by weight of water.
EP19940400801 1993-04-23 1994-04-13 Emulsifier for portable fire extinguishers Expired - Lifetime EP0621057B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9304821 1993-04-23
FR9304821 1993-04-23

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EP0621057A1 EP0621057A1 (en) 1994-10-26
EP0621057B1 true EP0621057B1 (en) 1996-11-13

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EP (1) EP0621057B1 (en)
JP (1) JP2575289B2 (en)
AU (1) AU658341B2 (en)
CA (1) CA2121654A1 (en)
DE (1) DE69400885T2 (en)
DK (1) DK0621057T3 (en)
ES (1) ES2094028T3 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
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KR101358249B1 (en) 2013-07-19 2014-02-06 혜정산업 (주) Eco-friendly afff fire-fighting composition
KR101366308B1 (en) 2013-07-19 2014-02-21 혜정산업 (주) Eco-friendly fire-fighting foam composition

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995012433A1 (en) * 1993-11-01 1995-05-11 Tyler, Robert, E. Fire fighting and cooling foam composition
FR2734737B1 (en) * 1995-06-01 1997-07-11 Seppic Sa FOAMING COMPOSITION AND ITS USE AS A FIRE-FIGHTING EMULSE
AU2830997A (en) * 1996-06-06 1998-01-05 Minnesota Mining And Manufacturing Company Fire-fighting agents containing adsorbable fluorocarbon surfactants
JP2001525234A (en) * 1997-12-10 2001-12-11 ミネソタ マイニング アンド マニュファクチャリング カンパニー Fire extinguisher containing adsorptive fluorocarbon surfactant
US6379578B1 (en) 1998-08-14 2002-04-30 Gtl Co., Ltd. Water-based foam fire extinguisher
JP3377450B2 (en) * 1998-08-14 2003-02-17 株式会社ジー・ティ・エル Water-based foam
FR2787721B1 (en) * 1998-12-24 2001-02-02 Atochem Elf Sa EXTINGUISHING COMPOSITIONS
WO2009080225A2 (en) * 2007-12-21 2009-07-02 Cognis Ip Management Gmbh Adjuvants for agrochemical applications
CA2813077A1 (en) 2010-10-01 2012-04-05 Tyco Fire Products Lp Aqueous fire-fighting foams with reduced fluorine content
BE1025603B1 (en) * 2018-02-06 2019-04-25 Uniteq S.A. EXTINGUISHING FOAM COMPOSITION
TW202035361A (en) * 2018-12-12 2020-10-01 美商3M新設資產公司 Fluorinated amine oxide surfactants
CN110478847B (en) * 2019-09-29 2021-08-13 中国科学技术大学 An environmentally friendly aqueous film-forming foam fire extinguishing agent based on short-chain fluorocarbons

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4090967A (en) * 1975-12-19 1978-05-23 Ciba-Geigy Corporation Aqueous wetting and film forming compositions
DE2732555C2 (en) * 1977-07-19 1982-07-01 Hoechst Ag, 6000 Frankfurt Fatty alcohol-free foam concentrate
US4999119A (en) * 1989-07-20 1991-03-12 Chubb National Foam, Inc. Alcohol resistant aqueous film forming firefighting foam

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101358249B1 (en) 2013-07-19 2014-02-06 혜정산업 (주) Eco-friendly afff fire-fighting composition
KR101366308B1 (en) 2013-07-19 2014-02-21 혜정산업 (주) Eco-friendly fire-fighting foam composition

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AU658341B2 (en) 1995-04-06
ES2094028T3 (en) 1997-01-01
JP2575289B2 (en) 1997-01-22
EP0621057A1 (en) 1994-10-26
DE69400885D1 (en) 1996-12-19
DK0621057T3 (en) 1997-04-28
AU6059594A (en) 1994-11-17
DE69400885T2 (en) 1997-05-15
JPH06312030A (en) 1994-11-08
CA2121654A1 (en) 1994-10-24

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