AEROSOL DEVICE DELIVERING A COMPOSITION BASED ON ETHYLENE OXIDE AND PROPYLENE OXIDE POLYCONDENSATE AND FIXING POLYMER

The aerosol device with ethylene oxide and propylene oxide polycondensates, fixing polymers, and solvents addresses non-homogeneous distribution and environmental concerns, achieving effective hair styling with pleasant feel and long-lasting hold.

FR3142884B1Active Publication Date: 2025-10-31LOREAL SA
View PDF 0 Cites 0 Cited by

Patent Information

Application Number
FR2022013065
Authority / Receiving Office
FR · FR
Patent Type
Patents
Current Assignee / Owner
Filing Date
2022-12-09
Publication Date
2025-10-31
Estimated Expiration
2042-12-09

AI Technical Summary

Technical Problem

Existing aerosol styling products for keratin fibers suffer from non-homogeneous distribution, unpleasant texture, insufficient fixing power, and environmental concerns due to propellant gases, failing to provide long-lasting styling and curl definition.

Method used

An aerosol device using a composition of ethylene oxide and propylene oxide polycondensates, fixing polymers, and solvents, delivered without propellant gas, utilizing a mechanical spraying system to achieve homogeneous distribution and pleasant feel, with good styling properties and reduced pressure.

Benefits of technology

The device delivers a continuous spray with small droplets, providing excellent hair hold, curl definition, and a natural appearance, while reducing environmental impact and extending device lifespan.

✦ Generated by Eureka AI based on patent content.
Patent Text Reader

Abstract

The present invention relates to an aerosol device comprising a keratin fiber coating composition that can be dispensed without a propellant gas, by mechanical spraying. The invention also relates to the use of the device and a method for treating keratin fibers implementing the device according to the invention.
Need to check novelty before this filing date? Find Prior Art

Description

Title of the invention: AEROSOL DEVICE DELIVERING A COMPOSITION BASED ON ETHYLENE OXIDE AND PROPYLENE OXIDE POLYCONDENSATE AND FIXING POLYMER

[0001] The present invention relates to an aerosol device comprising a keratin fiber coating composition which can be dispensed without propellant gas, by mechanical spraying.

[0002] The invention also relates to the use of the device and a method for treating keratin fibers implementing the device according to the invention.

[0003] Styling products are usually used to build, structure, and hold a hairstyle. They typically come in the form of lotions, gels, mousses, creams, sprays, etc., and are generally applied to hair, which is then styled before blow-drying or blow-drying.

[0004] However, currently known aerosol styling products do not give complete satisfaction, both in terms of the distribution of the styling product and the styling product itself.

[0005] In particular, the distribution of the styling product by an aerosol device is generally not sufficiently homogeneous or even. Furthermore, the texture of the styling product is not always pleasant, and the fixing power of the keratin fibers in these products is generally insufficient, particularly in terms of the longevity of the hair styling.

[0006] Furthermore, an increasing number of users of hair styling products are specifically looking for aerosol devices that do not use propellant gas. Indeed, most users have a negative image of propellant gases, often associating them with greenhouse gases that are harmful to the environment.

[0007] There is therefore a real need to develop an aerosol device that distributes homogeneously and regularly, without the use of propellant gas, a composition that gives a pleasant feel and provides good styling properties to keratin fibers, in particular good fixing power of keratin fibers and good persistence of the hairstyle over time.

[0008] These objectives are achieved with the present invention, which relates in particular to an aerosol device, devoid of a propellant, comprising: i. a composition comprising: a. one or more polycondensates of ethylene oxide and propylene oxide, preferably of formula (A): H-(O-CH2-CH2)a-(O-CH(CH3)-CH2)b-(O-CH2-CH2)a-OH (A) in which: a and a', whether identical or different, are integers between 2 and 150, and b is an integer between 1 and 100, b. one or more fixing polymer(s), and c. one or more solvents chosen from water, organic solvents, and their mixtures; ii. a container containing said composition; and iii. at least one mechanical spraying system for said composition.

[0009] The aerosol device according to the invention makes it possible to deliver the styling composition in the form of a continuous spray in a homogeneous and regular manner. The particle size of the spray is as small as that obtained with an aerosol composition comprising a propellant, despite a much lower pressure in the device according to the invention.

[0010] It has been observed that the composition delivered by the aerosol device according to the invention gives a particularly pleasant feel, in particular it does not give a "wetting effect" to the keratin fibers.

[0011] Furthermore, it has been observed that the composition delivered by the aerosol device according to the invention provides very good styling properties. In particular, the composition allows for good hold of the hair over time, both in wet and dry conditions, while adding volume to the hair, and without stiffening the style. In the case of curly hair, the composition according to the invention provides good curl definition.

[0012] In particular, the composition delivered by the aerosol device gives the hairstyle a natural appearance and allows for fluid movement. It also provides a particularly soft and pleasant feel to the hair.

[0013] The styling composition is delivered without the aid of a propellant agent, by the aerosol device according to the invention, which includes a mechanical pumping means. This means advantageously makes it possible to increase the pressure inside the container.

[0014] Furthermore, the device according to the invention has the advantage of being able to deliver the styling product in the form of a continuous spray with an average droplet size equivalent to that obtained with a propellant gas aerosol device, while having a reduced pressure inside the container (approximately 2 to 5 bar for the device according to the invention versus approximately 8 to 9 bar in a propellant gas aerosol device). This reduced pressure in the device according to the invention makes it possible, in particular, to reduce wear on the parts subjected to pressure, and therefore to increase the operating time of the device, but also to reduce the risks associated with storing products under pressure (for example, the risk of explosion during high-temperature storage).

[0015] The absence of a propellant also allows for easier refilling of the device with styling product, thus facilitating its reuse. The device according to the invention therefore has a reduced environmental impact compared to a conventional aerosol device with a propellant (which, moreover, generally cannot be refilled with styling product by the user).

[0016] The invention also relates to a method for treating keratin fibers comprising at least one step of spraying said keratin fibers with a composition, preferably cosmetic, by means of an aerosol device without a propellant agent.

[0017] The invention also relates to the use of the device according to the invention for the treatment, preferably the styling, of keratin fibers.

[0018] Other objects, features, aspects and advantages of the invention will become even clearer upon reading the description and example that follows.

[0019] In this description, and unless otherwise indicated: - the expression "at least one" is equivalent to the expression "one or more" and can be substituted for it; the expression "between" is equivalent to the expression "ranging from" and can be substituted for it, and implies that the bounds are included. - By the expression "greater than" and respectively the expression "less than" in the meaning of the present invention, we mean a closed interval, and therefore that the limits are included. - For the purposes of this application, "keratin fibers" means human keratin fibers and more specifically hair. - For the purposes of this invention, "polyoxyalkylated compound" means a compound comprising at least one polyoxyethylene and / or polyoxypropylene and / or polyglycerol group; preferably, the number of ethylene oxide and / or propylene oxide groups may range from 1 to 100, and the number of glycerol groups may range from 2 to 30. - By "non-polyoxyalkylated compound" in the sense of the present invention, we mean a compound not comprising several polyoxyethylene and / or polyoxypropylene and / or polyglycerol groups.

[0020] The composition contained in the device according to the invention

[0021] Polycondensates of ethylene oxide and propylene oxide The composition contained in the device according to the invention comprises one or more polycondensate(s) of ethylene oxide and propylene oxide, preferably of formula (A): H-(O-CH2-CH2)a-(O-CH(CH3)-CH2)b-(O-CH2-CH2)a-OH (A) in which: a and a', whether identical or different, are integers between 2 and 150, and b is an integer between 1 and 100.

[0022] Advantageously, the ethylene oxide and propylene oxide polycondensate of formula (A) corresponds to a triblock polyethylene glycol / polypropylene glycol / polyethylene glycol polycondensate.

[0023] Preferably, the integers a and a', identical or different, are between 2 and 130; more preferably between 5 and 130; more preferably still between 10 and 130.

[0024] More preferably, a and a' are identical.

[0025] Preferably, the integer b is between 2 and 80; more preferably between 10 and 80; more preferably still between 20 and 80.

[0026] According to a preferred embodiment of the invention: - the integers a and a', whether identical or different, are between 2 and 130; more preferably between 5 and 130; more preferably still between 10 and 130; and - the integer b is between 2 and 80; more preferably between 10 and 80; more preferably still between 20 and 80.

[0027] More preferably according to this embodiment of the invention, a and a' are identical.

[0028] Advantageously, the ethylene oxide and propylene oxide polycondensates usable in the composition according to the invention have an average molecular weight by weight ranging from 250 to 19,000, and better from 1,200 to 15,000, more preferably from 1,500 to 10,000, and even better from 1,500 to 5,000.

[0029] Advantageously, the ethylene oxide and propylene oxide polycondensates usable in the composition according to the invention have a cloudiness temperature, in a 10% by weight aqueous solution, greater than or equal to 20°C; preferably greater than or equal to 50°C. The cloudiness temperature can be measured according to ISO 1065.

[0030] Preferably, the composition contained in the device according to the invention comprises at least one polycondensate of ethylene oxide and propylene oxide of formula (A) selected from Poloxamer 108, Poloxamer 338, Poloxamer 124, Poloxamer 122, Poloxamer 407, Poloxamer 184, Poloxamer 238, Poloxamer 237, Poloxamer 188, and mixtures thereof; more preferably the polycondensate of ethylene oxide and propylene oxide is Poloxamer 184.

[0031] Among the ethylene oxide and propylene oxide polycondensates usable in the composition according to the invention, we can mention in particular the triblock polyethylene glycol / polypropylene glycol / polyethylene glycol polycondensates sold under the names "SYNPERONIC" such as "SYNPERONIC® PE / F32" (INCI name: POLOXAMER 108), "SYNPERONIC® PE / F108" (INCI name: POLOXAMER 338), "SYNPERONIC® PE / L44" (INCI name: POLOXAMER 124), "SYNPERONIC® PE / L42 (INCI name: POLOXAMER 122), "SYNPERONIC® PE / F127" (INCI name: POLOXAMER 407), "SYNPERONIC® PE / F88" (INCI name: POLOXAMER 238), "SYNPERONIC® PE / L64" (INCI name: POLOXAMER 184), "SYNPERONIC® PE / F88" (INCI name: POLOXAMER 238), "SYNPERONIC® PE / F87" (INCI name: POLOXAMER 237) by the company CRODA, or "LUTROL® F68" (INCI name: POLOXAMER 188) by the company BASF.

[0032] Preferably, the content of polycondensate(s) of ethylene oxide and propylene oxide present in the composition contained in the device according to the invention is in the range of 0.01 to 20% by weight, more preferably 0.1 to 10% by weight, better 0.5 to 5% by weight, and even better 0.75 to 3% by weight, relative to the total weight of said composition.

[0033] Preferably, the content of polycondensate(s) of ethylene oxide and propylene oxide of formula (A) in the composition contained in the device according to the invention is in the range of 0.01 to 20% by weight, more preferably 0.1 to 10% by weight, better 0.5 to 5% by weight, and even better 0.75 to 3% by weight, relative to the total weight of said composition.

[0034] Preferably, the Poloxamer(s) content in the composition contained in the device according to the invention is in the range of 0.01 to 20% by weight, more preferably 0.1 to 10% by weight, better 0.5 to 5% by weight, and even better 0.75 to 3% by weight, relative to the total weight of said composition.

[0035] Preferably, the Poloxamer 184 content in the composition contained in the device according to the invention is in the range of 0.01 to 20% by weight, more preferably 0.1 to 10% by weight, better 0.5 to 5% by weight, and even better 0.75 to 3% by weight, relative to the total weight of said composition.

[0036] Fixing polymers The composition contained in the device according to the invention comprises one or more fixing polymers.

[0037] For the purposes of the invention, "fixing polymer" means any polymer capable, by application to the hair, of giving the hair a shape or of allowing the maintenance of a shape already acquired.

[0038] All anionic, amphoteric, cationic, non-ionic fixing polymers and their mixtures, used in the technique can be used in the composition contained in the device according to the invention.

[0039] In particular, the fixing polymer(s) usable according to the invention can be chosen from non-ionic fixing polymers, anionic fixing polymers, cationic fixing polymers, amphoteric fixing polymers, and mixtures thereof.

[0040] Preferably, the fixing polymer(s) are chosen from among the fixing polymers non-ionic, anionic fixing polymers, amphoteric fixing polymers, and mixtures thereof.

[0041] More preferably, the fixing polymer(s) are chosen from anionic fixing polymers, non-ionic fixing polymers, and mixtures thereof.

[0042] More preferably, the fixing polymer(s) are chosen from among anionic fixing polymers.

[0043] The anionic fixing polymers usable in the composition contained in the device according to the invention are preferably polymers comprising groups derived from carboxylic, sulfonic or phosphoric acid and have a number average molecular mass of between about 500 and 5,000,000.

[0044] The carboxylic groups are provided by unsaturated mono- or dicarboxylic acid monomers such as those corresponding to formula (III): R, (in> - \ ---COOh R< % » in which n is an integer from 0 to 10, Ai denotes a methylene group, possibly linked to the carbon atom of the unsaturated group or to the neighboring methylene group when n is greater than 1, via a heteroatom such as oxygen or sulfur, R7 denotes a hydrogen atom, a phenyl or benzyl group, R8 denotes a hydrogen atom, a lower alkyl or carboxyl group, R9 denotes a hydrogen atom, a lower alkyl group, a -CH2-COOH, phenyl or benzyl group.

[0045] In the aforementioned formula, a lower alkyl group preferably designates a group having 1 to 4 carbon atoms and in particular, the methyl and ethyl groups.

[0046] Preferred anionic fixing polymers with carboxylic groups according to the invention are: A) Acrylic or methacrylic acid copolymers or their salts. Among these polymers are copolymers of acrylic or methacrylic acid with a monoethylenic monomer such as ethylene, styrene, vinyl esters, or acrylic or methacrylic acid esters, possibly grafted onto a polyalkylene glycol such as polyethylene glycol, and possibly crosslinked. Such polymers are described in particular in French patent no. 1222944 and German patent application no. 2330956. Copolymers of this type have in their chain an acrylamide unit, possibly N-alkylated and / or hydroxyalkylated, as described in particular in Luxembourg patent applications nos. 75370 and 75371. Also noteworthy are C1-C4 copolymers of acrylic acid and alkyl methacrylate. and vinylpyrrolidone, acrylic acid, and C1-C20 alkyl methacrylate terpolymers, for example, lauryl methacrylate, such as that marketed by ISP under the name ACRYLIDONE® LM (INCI name VP / acrylates / lauryl methacrylate copolymer), acrylic acid / ethyl acrylate / nt-butylacrylamide terpolymers such as the products ULTRAHOLD® STRONG and ULTRAHOLD® 8 marketed by BASF (INCI name Acrylates / t-butylacrylamide copolymer), methacrylic acid / ethyl acrylate / tert-butyl acrylate terpolymers such as the products marketed under the names LUVIMER® 100 P or LUVIMER® PRO 55 by BASF (INCI name Acrylates copolymer), copolymers of methacrylic and ethyl acrylate such as the products marketed under the names LUVIMER® MAE or LUVIFLEX® SOFT by BASF (INCI name Acrylates copolymer),Acrylic acid / butyl acrylate / methyl methacrylate terpolymers, such as the product marketed under the name BALANCE® CR by AKZO NOBEL (INCI name Acrylates copolymer), and methacrylic acid and methyl methacrylate copolymers sold under the name EUDRAGIT® L 100 by ROHM PHARMA (INCI name Acrylates copolymer). Also included are branched sequence polymers containing (meth)acrylic acid monomers, such as the product sold under the name FIXATE® G-100L by LUBRIZOL (INCI name AMP-acrylates / allyl methacrylate copolymer). B) Crotonic acid copolymers, such as those containing in their chain vinyl acetate or propionate motifs, and possibly other monomers such as allylic or methallylic esters, vinyl ether or vinyl ester of a saturated linear or branched, long-chain hydrocarbon carboxylic acid, such as those containing at least 5 carbon atoms, these polymers possibly being grafted or crosslinked, or another vinyl ester, allylic or methallylic monomer of an α- or α-cyclic carboxylic acid. Such polymers are described among others in French patents nos. 1222944, 1580545, 2265782, 2265781, 1564110 and 2439798. Commercial products falling into this class are produced RESYN® 28-2930 and 28-1310 marketed by the company AKZO NOBEL (INCI names: VA / crotonates / vinyldecanoate copolymer and VA / crotonates copolymer respectively).We can also mention the products LUVISET® CA 66 sold by BASF, ARISTOFLEX® A60 sold by CLARIANT (INCI name VA / crotonates copolymer) and MEXOMERE® PW or PAM sold by CHIMEX (INCI name VA / vinyl butyl benzoate / crotonates copolymer). C) Copolymers of monounsaturated C4-C8 carboxylic acids or anhydrides Choose from: - copolymers comprising (i) one or more maleic, fumaric, itaconic acids or anhydrides and (ii) at least one monomer selected from vinyl esters, vinyl ethers, vinyl halides, phenylvinyl derivatives, acrylic acid and its esters, the anhydride functions of these copolymers optionally being monoesterified or monoamidified. Such polymers are described in particular in US patents 2047398, 2723248, 2102113, and patent GB839805. Commercial products include those sold under the names GANTREZ® AN or ES by the company ISP, such as GANTREZ® ES 225 (INCI name Ethyl ester of PVM / MA copolymer) or GANTREZ® ES 425L (INCI name Butyl ester of PVM / MA copolymer); - copolymers comprising (i) one or more maleic, citraconic, itaconic anhydride motifs and (ii) one or more monomers selected from al-lylic or methallylic esters possibly comprising one or more acrylamide, methacrylamide, α-olefin, acrylic or methacrylic esters, acrylic or methacrylic acid or vinylpyrrolidone groups in their chain, the anhydride functions of these copolymers possibly being monoesterified or monoamidified. These polymers are described for example in patents FR2350384 and FR2357241. D) Polyacrylamides containing carboxylate groups.

[0047] The fixing polymers with motifs derived from sulfonic acid can be selected from A') Homopolymers and copolymers containing vinylsulfonic, styrene-sulfonic, naphthalene-sulfonic or acrylamido-alkylsulfonic motifs. These polymers can be chosen from, among others: - salts of polyvinylsulfonic acid having a molecular mass between about 1,000 and 100,000, as well as copolymers with an unsaturated comonomer such as acrylic or methacrylic acids and their esters, as well as acrylamide or its derivatives, vinyl ethers and vinylpyrrolidone; - polystyrene-sulfonic acid salts such as sodium salts sold for example under the name FLEXAN® II by AKZO NOBEL (INCI name Sodium polystyrene sulfonate). These compounds are described in patent FR 2198719; - polyacrylamide-sulfonic acid salts such as those mentioned in US patent 4128631, and more particularly polyacrylamidoethylpropane-sulfonic acid sold under the name RHEOCARE® HSP-1180 by COGNIS (INCI name polyacrylamidomethylpropane sulfonic acid). B') Sulfonylated polyesters, these polymers being advantageously obtained by polycondensation of at least one dicarboxylic acid, at least one diol, or a A mixture of a diol and a diamine, and at least one difunctional monomer containing a sulfonic acid group. Examples of such polymers include: - linear sulfonic polyesters such as those described in patent applications US 3734874, US 3779993, US 4119680, US 4300580, US 4973656, US 5660816, US 5662893 and US 5674479. Such polymers are for example the products EASTMAN® AQ38S POLYMER, EASTMAN® AQ55S POLYMER, EASTMAN® AQ48 ULTRA POLYMER marketed by the company EASTMAN CHEMICAL (name Polyester-5) which are copolymers obtained from diethylene glycol, 1,4-cyclohexanedimethanol, isophthalic acid and salt of sulfoisophthalic acid. - Branched sulfonic polyesters such as those described in patent applications WO 95 / 18191, WO 97 / 08261 and WO 97 / 20899. Such compounds are for example the products EASTMAN® AQ10D POLYMER (designation Polyester-13) or EASTMAN® AQ1350 POLYMER offered by the company EASTMAN CHEMICAL (designation Polyester-13).

[0048] According to the invention, the anionic fixing polymers are preferably selected from acrylic acid copolymers such as acrylic acid / ethyl acrylate / N-tert-butylacrylamide terpolymers sold in particular under the name ULTRAHOLD® STRONG by BASF, crotonic acid derived copolymers such as vinyl acetate / vinyl tert-butylbenzoate / crotonic acid terpolymers and crotonic acid / vinyl acetate / neododecanoate terpolymers sold in particular under the name RESYN 28-2930 by AKZO NOBEL, polymers derived from maleic, fumaric, itaconic acids or anhydrides with vinyl esters, vinyl ethers, vinyl halides, phenyl vinyl derivatives, acrylic acid and its esters such as copolymers methyl vinyl ether / maleic anhydride monoesterified sold, for example, under the names GANTREZ® ES 425L or ES 225 by the company ISP,methacrylic acid and ethyl acrylate copolymers sold under the name LUVIMER® MAE by BASF, vinyl acetate / crotonic acid copolymers sold under the name LUVISET® CA 66 by BASF, polyethylene glycol-grafted vinyl acetate / crotonic acid copolymers sold under the name ARISTOFLEX® A60 by CLARIANT, vinylpyrrolidone / acrylic acid / lauryl methacrylate terpolymers sold under the name ACRYLIDONE® LM by ISP, the polymer sold under the name FIXATE® G-100L by LUBRIZOL, vinyl acetate / crotonic acid / vinyl p-tert-butylbenzoate copolymers sold under the names MEXOMERE® PW or PAM by Chimex.

[0049] The amphoteric fixing polymers usable in the composition contained in the device according to the invention are preferably chosen from polymers comprising motifs B and C statistically distributed in the polymer chain where B designates a motif derived from a monomer comprising at least one basic nitrogen atom and C designates a motif derived from an acidic monomer comprising one or more carboxylic or sulfonic groups, or B and C may designate groups derived from zwitterionic monomers of carboxybetaines or sulfobetaines; B and C can also refer to a cationic polymer chain comprising primary, secondary, tertiary or quaternary amine groups, in which at least one of the amine groups bears a carboxylic or sulfonic group linked via a hydrocarbon group, or B and C are part of a chain of an ethylene-α,[3-dicarboxylic motif polymer in which one of the carboxylic groups has been made to react with a polyamine comprising one or more primary or secondary amine groups.

[0050] Amphoteric fixing polymers meeting the above definition are particularly preferred and selected from the following polymers: (1) Copolymers with acidic and basic vinyl motifs, such as those resulting from the copolymerization of a monomer derived from a vinyl compound bearing a carboxyl group, such as, more particularly, acrylic acid, methacrylic acid, maleic acid, alpha-chloroacrylic acid, and a basic monomer derived from a substituted vinyl compound containing at least one basic atom, such as, more particularly, dialkylaminoalkyl methacrylate and acrylate, dialkylaminoalkylmethacrylamide, and acrylamide. Such compounds are described in U.S. Patent No. 3836537. (2) polymers containing derived motifs: a) of at least one monomer chosen from acrylamides or methacrylamides substituted on the nitrogen atom by an alkyl group, b) of at least one acidic comonomer containing one or more reactive carboxylic groups, and c) of at least one basic comonomer such as primary, secondary, tertiary and quaternary amine-substituting esters of acrylic and methacrylic acids, and the quaternization product of dimethylaminoethyl methacrylate with dimethyl or diethyl sulfate. The N-substituted acrylamides or methacrylamides most particularly preferred according to the invention are compounds whose alkyl groups comprise from 2 to 12 carbon atoms, and more particularly N-ethylacrylamide, N-tert-butylacrylamide, N-tert-octylacrylamide, N-octylacrylamide, N-decylacrylamide, N-dodecylacrylamide and the corresponding methacrylamides. The acid comonomers are chosen more particularly from acrylic, methacrylic, crotonic, itaconic, maleic, fumaric acids as well as alkyl monoesters having 1 to 4 carbon atoms of maleic or fumaric acids or anhydrides. Preferred basic comonomers are aminoethyl, butylaminoethyl, N,N'-dimethylaminoethyl, and N-tert-butylaminoethyl methacrylates. Copolymers with the INCI name Octyla-crylamide / acrylates / butylaminoethyl methacrylate copolymer are particularly used, such as the products sold under the names AMPHOMER®, AMPHOMER® LV71 or BALANCE® 47 by the company AKZO NOBEL. (3) crosslinked and acylated polyaminoamides partially or totally derived from polyaminoamides of general formula (IV): . .. . .. .... -, ; (IV) in which Rio represents a divalent group derived from a saturated dicarboxylic acid, a mono- or dicarboxylic aliphatic acid with an ethylenic double bond, an ester of a lower alkanol having 1 to 6 carbon atoms of these acids, or a group derived from the addition of any of said acids with a bis-primary or bis-secondary amine, and Z denotes a group derived from a bis-primary, mono- or bis-secondary polyalkylene-polyamine and preferably represents: a) in proportions of 60 to 100% by mole, group (V) ..................W H * s H where x=2 and p=2 or 3, or x=3 and p=2 this group derived from diethylenetriamine, triethylenetetraamine or dipropylenetriamine; b) in proportions of 0 to 40% by moles, the group (V) above, in which x=2 and p=l and which is derived from ethylenediamine, or the group derived from piperazine: c) in proportions of 0 to 20% by mole, the -NH-(CH2)e-NH- group derived from hexamethylenediamine, these polyaminoamides being crosslinked by the addition reaction of a bifunctional crosslinking agent chosen from epihalohydrins, diepoxides, dianhydrides, bis-unsaturated derivatives, using 0.025 to 0.35 mole of crosslinking agent per amine group of the polyaminoamide, and acylated by the action of acrylic acid, chloroacetic acid or an alkane-sultone or their salts. Saturated carboxylic acids are preferably chosen from acids with 6 to 10 carbon atoms such as adipic, 2,2,4-trimethyl and 2,4,4-trimethyl, terephthalic acids, and ethylenic double-bonded acids such as acrylic, methacrylic, and itaconic acids. The alkane-sultones used in acylation are preferably propane- or butane-sultone, the salts of the acylation agents are preferably sodium or potassium salts. (4) polymers having zwitterionic motifs of formula (VI): in which Ru denotes a polymerizable unsaturated group such as an acrylate, methacrylate, acrylamide or methacrylamide group, y and z represent an integer from 1 to 3, Rn and Rn represent a hydrogen atom, a methyl, ethyl or propyl group, R[4 and Ri5 represent a hydrogen atom or an alkyl group such that the sum of the carbon atoms in R[4 and Ri5 does not exceed 10. Polymers comprising such motifs may also include motifs derived from non-zwitterionic monomers such as dimethyl- or diethyl-aminoethyl acrylate or methacrylate or alkyl acrylates or methacrylates, acrylamides or methacrylamides, or vinyl acetate. As an example, we can cite methyl methacrylate / dimethyl-carboxymethylammonio-ethyl methyl methacrylate copolymers, such as the product sold under the name DIAFORMER Z-301N or Z-301W by the company CLARIANT (INCI name Acrylates copolymer). (5) chitosan-derived polymers comprising monomer units conforming to the following formulas (D), (E) and (F): motif (D) being present in proportions between 0 and 30%, motif (E) in proportions between 5 and 50% and motif (F) in proportions between 30 and 90%, it being understood that in this motif (F), R[6] represents a formula group (VII): R.„ (VII) ! —C—((¾-G in which: if q=0, Rn, Rn and Rn, identical or different, each represent a hydrogen atom, a methyl, hydroxyl, acetoxy or amino residue, a monoalkylamine residue or a dialkylamine residue possibly interrupted by one or more nitrogen atoms and / or possibly substituted by one or more amine, hydroxyl, carboxyl, alkylthio, sulfonic groups, an alkylthio residue whose alkyl group bears an amino residue, at least one of the groups Rn, Rn and Rn being in this case a hydrogen atom; or if q=l, Rlb Rn and Rn each represent a hydrogen atom, as well as the salts formed by these compounds with bases or acids. (6) Polymers containing motifs conforming to the general formula (VIII) are, for example, described in French patent FR 1400366: in which R20 represents a hydrogen atom, a CH3O-, CH3CH2O-, phenyl group, R2i denotes a hydrogen atom or a lower alkyl group such as methyl, ethyl, R22 denotes a hydrogen atom or a lower alkyl group in Ci-C6 such as methyl, ethyl, R23 denotes a lower alkyl group in Ci-C6 such as methyl, ethyl or a group corresponding to the formula: -R24-N(R22)2, R24 representing a -CH2-CH2-, -CH2-CH2-CH2, -CH2-CH(CH3)- group, R22 having the meanings mentioned above. (7) Polymers derived from the N-carboxyalkylation of chitosan such as N-carboxymethyl-chitosan or N-carboxybutyl-chitosan, such as for example the product sold under the name CHITOGLYCAN by the company SINERGA SPA (INCI name: Carboxymethyl chitosan). (8) Amphoteric polymers of the -DXDX type selected from: a) polymers obtained by the action of chloroacetic acid or sodium chloroacetate on compounds having at least one motif of formula (IX): -DXDXD- (IX) where D denotes a group and X designates the symbol E or E', E or E' identical or different designate a divalent group which is a straight or branched alkylene group, comprising up to 7 carbon atoms in the main chain unsubstituted or substituted by hydroxyl groups and may further comprise oxygen, nitrogen, sulfur atoms, 1 to 3 aromatic and / or heterocyclic rings; the oxygen, nitrogen and sulfur atoms being present as ether, thioether, sulfoxide, sulfone, sulfonium, alkylamine, alkenylamine, hydroxyl, benzylamine, amine oxide, quaternary ammonium, amide, imide, alcohol, ester and / or urethane groups. b) Polymers with formula (X): -DXDX- (X) where D denotes a group and X denotes the symbol E or E' and at least once E'; E having the meaning indicated above and E' is a divalent group which is a straight or branched chain alkylene group, having up to 7 carbon atoms in the main chain, substituted or not by one or more hydroxyl groups and comprising one or more nitrogen atoms, the nitrogen atom being substituted by an alkyl chain possibly interrupted by an oxygen atom and necessarily comprising one or more carboxyl functions or one or more hydroxyl functions and betainized by reaction with chloroacetic acid or sodium chloroacetate. (9) Alkyl(Ci-C5)->vinyl ether / maleic anhydride copolymers partially modified by semiamidification with an N,N-dialkylaminoalkylamine such as N,N-dimethylaminopropylamine or by semiesterification with an N,N-dialkylaminoalkanol. These copolymers may also contain other vinyl comonomers such as vinylcaprolactam.

[0051] Among the amphoteric fixing polymers mentioned above that are particularly preferred according to the invention, those of family (3) such as copolymers of which

[0052]

[0053] The INCI name is Octylacrylamide / acrylates / butylamino ethylmethacrylate copolymer, such as the products sold under the names AMPHOMER®, AMPHOMER® LV 71 or BALANCE® 47 by the company AKZO NOBEL and those of the family (4) such as the methyl methacrylate / dimethyl-carboxymethylammonio-ethyl methyl methacrylate copolymers sold for example under the name DIAFORMER Z-301N or Z-301W by the company CLARIANT. The cationic fixing polymers usable in the composition contained in the device according to the invention are preferably chosen from polymers comprising primary, secondary, tertiary and / or quaternary amine groups forming part of the polymer chain or directly linked thereto, and having a molecular weight between 500 and about 5,000,000 and preferably between 1,000 and 3,000,000. Among these polymers, the following cationic polymers are particularly noteworthy: (1) homopolymers or copolymers derived from acrylic or methacrylic esters or amides and comprising at least one of the following formula units: in which: R3 designates a hydrogen atom or a CH3 group; A is a linear or branched alkyl group consisting of 1 to 6 carbon atoms or a hydroxyalkyl group consisting of 1 to 4 carbon atoms; R4, R5, R6, whether identical or different, represent an alkyl group having from 1 to 18 carbon atoms or a benzyl group; Ri and R2, whether identical or different, each represent a hydrogen atom or an alkyl group having from 1 to 6 carbon atoms; X denotes a methosulfate anion or a halide such as chloride or bromide. The copolymers of family (1) further contain one or more motifs derived from comonomers that can be selected from the families of acrylamides, methacrylamides, diacetone acrylamides, acrylamides and substituted methacrylamides. nitrogen by C1-C4 alkyl groups, groups derived from acrylic or methacrylic acids or their esters, vinyllactams such as vinylpyrrolidone or vinylcaprolactam, vinyl esters. Thus, among these copolymers of family (1), we can mention: - copolymers of acrylamide and quaternized dimethyl-amino-ethyl methacrylate with dimethyl sulfate or with a dimethyl halide, such as that sold under the name HERCOFLOC® by the company HERCULES, - acrylamide and methacryloyloxyethyltrimethylammonium chloride copolymers described for example in patent application EP-A-080976 and sold under the name BINA QU AT P 100 by the company CIBA GEIGY, - the copolymer of acrylamide and methacryloyloxy-ethyl-trimethyl-ammonium methosulfate such as that sold under the name RETEN by the company HERCULES, - vinylpyrrolidone / acrylate or dialkyl-amino-alkyl methacrylate copolymers, whether quantified or not, such as products sold under the name “GAFQUAT®” by the company ISP, such as “GAFQUAT® 734” or “GAFQUAT® 755” or the products named “COPOLYMER® 845, 958 and 937”. These polymers are described in detail in French patents 2,077,143 and 2,393,573. - fatty chain polymers with a vinylpyrrolidone motif, such as the products sold under the names Stylèze W20 and Stylèze W10 by ISP, - dimethylaminoethyl methacrylate / vinyl-capro-lactam / vinylpyrrolidone terpolymers such as the product marketed under the name GAFFIX VC 713 by ISP, and - and quaternized dimethyl-amino-propyl vinylpyrrolidone / methacrylamide copolymers such as the products marketed under the name "GAFQUAT® HS 100" by the company ISP. (2) Cationic guar gums, preferably quaternary ammonium guar gums such as those described in U.S. patents 3,589,578 and 4,031,307, such as guar gums containing trialkylammonium cationic groups. Such products are marketed, in particular, under the trade names JAGUAR C13 S, JAGUAR C 15, and JAGUAR C 17 by the company MEYHALL. (3) quaternary copolymers of vinylpyrrolidone and vinylimidazole; (4) chitosans or their salts; the usable salts are in particular chitosan acetate, lactate, glutamate, gluconate or pyrrolidone-carboxylate. Among these compounds, we can mention chitosan with a deacetylation rate of 90.5% by weight, sold under the name KYTAN BRUT STANDARD by the ABER TECHNOLOGIES company, chitosan pyrrolidone-carboxylate marketed under the name KYTAMER® PC by the company AMERCHOL. (5) cationic cellulose derivatives such as cellulose copolymers or cellulose derivatives grafted with a water-soluble monomer comprising a quaternary ammonium, and described in particular in US patent 4,131,576, such as hydroxyalkyl celluloses, such as hydroxymethyl-, hydroxyethyl- or hydroxypropyl celluloses grafted in particular with a salt of methacryloyloxyethyl trimethyl-lammonium, methacrylamidopropyl trimethylammonium, dimethyl-diallylammonium. The marketed products meeting this definition are more specifically the products sold under the name "CELQUAT L 200" and "CELQUAT H 100" by the National Starch Company.

[0054] The non-ionic fixing polymers usable in the composition contained in the device according to the invention are preferably chosen, for example, from: - polyalkyloxazolines; - vinyl acetate homopolymers; - vinyl acetate copolymers such as, for example, vinyl acetate and acrylic ester copolymers, vinyl acetate and ethylene copolymers, or vinyl acetate and maleic ester copolymers, for example, dibutyl maleate; - homopolymers and copolymers of acrylic esters such as, for example, alkyl acrylate and alkyl methacrylate copolymers such as the products offered by ROHM GmbH under the name EUDRAGIT® NE 30 D (INCI name Acrylates copolymer); - copolymers of acrylonitrile and a non-ionic monomer chosen, for example, from butadiene and alkyl (meth)acrylates; - styrene homopolymers; - styrene copolymers such as styrene, alkyl methacrylate and alkyl acrylate copolymers; styrene and butadiene copolymers; or styrene, butadiene and vinylpyridine copolymers; - polyamides; - vinyllactam homopolymers such as vinylpyr-rolidone homopolymers marketed for example under the names LUVISKOL® K30 powder by BASF or PVP K30L or K60 solution or K90 by ISP, or such as polyvinylcaprolactam marketed under the name LUVISKOL ® PLUS by BASF (INCI name PVP); - vinyllactam copolymers such as a poly(vinylpyrrolidone / vinyllactam) copolymer sold under the trade name LUVITEC® VPC 55K65W by BASF, poly(vinylpyrrolidone / vinyl acetate) copolymers such as those marketed under the name PVP / VA® S630L, E735, E635, W735 by ISP, LUVISKOL® VA 73, VA 64, VA 37 by BASF (INCI name VP / VA copolymer); and vinylpyrrolidone / methacrylamide / vinylimidazole terpolymers such as the one marketed under the name LUVISET® CLEAR by BASF (INCI name VP / methacrylamide / vinylimidazole copolymer). The alkyl groups of the non-ionic polymers mentioned above preferably have 1 to 6 carbon atoms.

[0055] According to the invention, grafted silicone-type fixing polymers can also be used, comprising a polysiloxane part and a part consisting of a non-siliconized organic chain, one of the two parts constituting the main chain of the polymer and the other being grafted onto said main chain.

[0056] These polymers are described for example in patent applications EP-A-0412704, EP-A-0412707, EP-A-0640105 and WO 95 / 00578, EP-A-0582152 and WO 93 / 23009 and US patents 4,693,935, US 4,728,571 and US 4,972,037.

[0057] These polymers can be amphoteric, cationic, anionic or non-ionic, and they are preferably anionic or non-ionic.

[0058] Such polymers are, for example, copolymers that can be obtained by radical polymerization from the mixture of monomers formed: a) 50 to 90% by weight of tert-butyl acrylate, b) 0 to 40% by weight of acrylic acid, c) 5 to 40% by weight of a silicone macromer of formula r 1 O CIL CH. CH. h ] " ! ' M " CHU —C ~C~0^(CH4. —-Si —Cf-Si. —CH? . ( ... . ( . ... Ci H CH. CH. Ci L , L ■■ Jy . where v is a number from 5 to 700, the weight percentages being calculated relative to the total weight of the monomers.

[0059] Other examples of grafted silicone polymers include polydimethylsiloxanes (PDMS) onto which are grafted, via a thiopropylene-type linker, mixed polymer motifs of the poly((meth)acrylic acid) and poly((meth)acrylate) type, and polydimethylsiloxanes (PDMS) onto which are grafted, via a thiopropylene-type linker, polymer motifs of the poly(meth)acrylate type of isobutyl.

[0060] For example, grafted silicone polymers are marketed under the names SILICONE PLUS POLYMER® VS80 and VA70 by 3M (names INCI Polysilicone-8 and Polysilicone-7 respectively).

[0061] As another type of silicone fixing polymer, we can mention the product LUVIFLEX® SILK marketed by BASF (INCI name PEG / PPG-25 / 25 dimethicone / acrylates Copolymer).

[0062] Functionalized or non-functionalized, silicone-coated or non-siliconized, non-ionic, anionic, cationic or amphoteric polyurethanes, or mixtures thereof, can also be used as fixing polymers.

[0063] The polyurethanes particularly targeted by the present invention are those described in applications EP 0 751 162, EP 0 637 600, EP 0 648 485 and FR 2 743 297 of which the applicant is the holder, as well as in applications EP 0 656 021 and WO 94 / 03510 of BASF, and EP 0 619 111 of National Starch.

[0064] As polyurethanes that are particularly suitable in the present invention, we can cite the products marketed under the names LUVISET PUR® and LUVISET® Si PUR by the company BASF (INCI names Polyurethane-1 and Polyurethane-6 respectively).

[0065] Preferably, the composition contained in the device according to the invention comprises at least one fixing polymer selected from non-ionic fixing polymers, anionic fixing polymers, and mixtures thereof; more preferably selected from anionic fixing polymers; more preferably selected from anionic fixing polymers with carboxylic groups; better selected from crotonic acid copolymers, such as those having vinyl acetate or propionate motifs in their chain, and optionally other monomers such as allylic or methallylic esters, vinyl ether or vinyl ester of a saturated, linear or branched, long hydrocarbon chain carboxylic acid, such as those having at least 5 carbon atoms, these copolymers possibly being grafted or crosslinked, or another vinyl ester, allylic or methallylic monomer of an α- or β-cyclic carboxylic acid;and even better chosen from among the Vinyl Acetate / Crotonates / Vinyl Neodecanoate copolymers, the Vinyl Acetate / Crotonates / Vinyl Decanoate copolymers, the Vinyl Acetate / Crotonates copolymers, the Vinyl Acetate / Vinyl Butyl Benzoate / Crotonates copolymers, and mixtures thereof. ;

[0066] In a particularly preferred manner, the composition contained in the device according to the invention comprises at least one Vinyl Acetate / Crotonates / Vinyl Neodecanoate copolymer.

[0067] Preferably, the content of fixing polymer(s) in the composition contained in the device according to the invention is in the range of 0.1 to 25% by weight, more preferably 0.5 to 20% by weight, more preferably still 1 to 15% by weight, better 2 to 10% by weight, and even better 3 to 8% by weight, relative to the total weight of said composition.

[0068] Preferably, the content of anionic fixing polymer(s) in the composition contained in the device according to the invention is in the range of 0.1 to 25% by weight, more preferably 0.5 to 20% by weight, more preferably still 1 to 15% by weight, better 2 to 10% by weight, and even better 3 to 8% by weight, relative to the total weight of said composition.

[0069] Preferably, the content of anionic fixing polymer(s) with carboxylic groups in the composition contained in the device according to the invention is in the range of 0.1 to 25% by weight, more preferably 0.5 to 20% by weight, more preferably still 1 to 15% by weight, better 2 to 10% by weight, and even better 3 to 8% by weight, relative to the total weight of said composition.

[0070] Preferably, the content of anionic fixing polymer(s) of the crotonic acid copolymer type in the composition contained in the device according to the invention is in the range of 0.1 to 25% by weight, more preferably 0.5 to 20% by weight, more preferably 1 to 15% by weight, better 2 to 10% by weight, and even better 3 to 8% by weight, relative to the total weight of said composition.

[0071] Preferably, the content of Vinyl Acetate / Crotonates / Vinyl Neo-decanoate copolymer(s) in the composition contained in the device according to the invention is in the range of 0.1 to 25% by weight, more preferably 0.5 to 20% by weight, more preferably still 1 to 15% by weight, better 2 to 10% by weight, and even better 3 to 8% by weight, relative to the total weight of said composition.

[0072] Solvents The composition contained in the device according to the invention comprises one or more solvents selected from water, organic solvents, and mixtures thereof.

[0073] Preferably, the solvent(s) are chosen from among organic solvents.

[0074] More preferably, the solvent(s) are chosen from among the C2-C8 alcohols.

[0075] For the purposes of the present invention, "C2-C8 alcohols" refers to mono-alcohols C2-C8 and C2-C8 polyols.

[0076] The organic solvent(s) usable in the composition contained in the device according to the invention are cosmetically acceptable.

[0077] By way of example, organic solvents may be chosen from C1-C4 alcohols, such as ethanol, isopropanol, tert-butanol or n-butanol; polyols (other than polycondensates a.); aromatic alcohols such as benzyl alcohol; and mixtures thereof.

[0078] For the purposes of this invention, "polyol" means an organic compound consisting of a hydrocarbon chain optionally interrupted by one or more oxygen atoms and carrying at least two free hydroxyl groups (-OH) on different carbon atoms, this compound can be cyclic or acyclic, linear or branched, saturated or unsaturated, and in the liquid state at room temperature (25°C) and atmospheric pressure.

[0079] Preferably, the polyol(s) according to the invention are acyclic and non-aromatic.

[0080] The polyols according to the invention comprise in their structure a number of carbon atoms ranging from 2 to 8, more preferably from 2 to 6, better from 2 to 5.

[0081] More particularly, the usable polyol(s) comprise from 2 to 10 hydroxy groups, more preferably from 2 to 5 hydroxy groups, more preferably still from 2 to 3 hydroxy groups.

[0082] Preferably, the usable polyol(s) are chosen from polyols comprising at least three carbon atoms and ethylene glycol, preferably are chosen from propylene glycol, 1,3-propanediol, 1,3-butylene glycol, pentane-1,2-diol, dipropylene glycol, hexylene glycol, pentylene glycol, glycerol, ethylene glycol, and a mixture of these compounds.

[0083] More preferably, the solvent(s) are chosen from among C2-C6 mono-alcohols and C2-C6 polyols.

[0084] Better still, the solvent(s) are chosen from among the mono-alcohols in C2-C6, and even better in C2-C4.

[0085] Even better, the solvent is ethanol.

[0086] In a particularly preferred manner, the composition contained in the device according to the invention comprises at least ethanol.

[0087] Preferably, the organic solvent(s) content in the composition contained in the device according to the invention is in the range of 10 to 99% by weight, more preferably 30 to 98% by weight, more preferably 50 to 97% by weight, and even better 70 to 95% by weight, relative to the total weight of said composition.

[0088] Preferably, the content of C2-C8 alcohol(s) in the composition contained in the device according to the invention is in the range of 10 to 99% by weight, more preferably 30 to 98% by weight, more preferably 50 to 97% by weight, and even better 70 to 95% by weight, relative to the total weight of said composition.

[0089] Preferably, the content of C2-C6 mono-alcohol(s) in the composition contained in the device according to the invention is in the range of 10 to 99% by weight, more preferably 30 to 98% by weight, more preferably 50 to 97% by weight, and even better 70 to 95% by weight, relative to the total weight of said composition.

[0090] Preferably, the ethanol content in the composition contained in the device according to the invention, is included in the range of 10 to 99% by weight, more preferably 30 to 98% by weight, more preferably 50 to 97% by weight, and even better 70 to 95% by weight, relative to the total weight of said composition.

[0091] The composition contained in the device according to the invention may include water.

[0092] When the composition includes water, the water content in the composition contained in the device according to the invention is preferably in the range of 10 to 99% by weight, more preferably 30 to 98% by weight, more preferably 50 to 97% by weight, and even better 70 to 95% by weight, relative to the total weight of said composition.

[0093] According to a preferred embodiment of the invention, the water content in the composition contained in the device is less than 10% by weight; preferably less than 5% by weight; more preferably less than 1% by weight; more preferably less than 0.5% by weight; better still less than 0.1% by weight, relative to the total weight of said composition.

[0094] Silicones The composition contained in the device according to the invention may optionally further comprise at least one silicone.

[0095] By "silicone" is meant all organosilicon polymers or oligomers with linear or cyclic, branched or cross-linked structure, of variable molecular weight, obtained by polymerization and / or polycondensation of suitably functionalized silanes, and consisting essentially of a repetition of principal motifs in which silicon atoms are linked together by oxygen atoms (siloxane bond -Si-O-Si-), with hydrocarbon radicals possibly substituted, being directly linked via a carbon atom to said silicon atoms; and more particularly dialkylsiloxane polymers, amino silicones, dimethiconols.

[0096] Preferably, the silicone(s) are chosen from polydialkylsiloxanes, in particular polydimethylsiloxanes (PDMS), and organo-modified polysiloxanes comprising at least one functional group chosen from amine groups, oxyalkylated groups, aryl groups and alkoxy groups.

[0097] Organopolysiloxanes are defined in more detail in Walter Noll's "Chemistry and Technology of Silicones" (1968), Academy Press. They can be volatile or non-volatile.

[0098] The non-volatile silicones usable in the composition according to the invention may preferably be non-volatile polydialkylsiloxanes, polyorganosiloxanes modified by organofunctional groups selected from among amine groups, aryl groups, oxyalkylated groups and groups alkoxy and their mixtures.

[0099] These silicones are more specifically chosen from among the polydialkylsiloxanes, among which the main examples are polydimethylsiloxanes with trimethylsilyl terminal groups. The viscosity of the silicones is measured at 25°C according to ASTM 445 Appendix C.

[0100] Among these polydialkylsiloxanes, the following commercial products may be cited by way of non-limiting example: - SILBIONE® oils from series 47 and 70 047 or MIRASIL® oils marketed by RHODIA; - the MIRASIL® series oils marketed by the company RHODIA; - oils from the 200 series of the DOW CORNING company; - VISCASIL® oils from GENERAL ELECTRIC and certain oils from the SF series (SF 96, SF 18) from GENERAL ELECTRIC.

[0101] We can also mention polydimethylsiloxanes with terminal dimethylsilanol groups known as dimethiconol (CTFA), such as the oils in the 48 series from the RHODIA company.

[0102] Organomodified silicones usable according to the invention are silicones as defined above and comprising in their structure one or more organofunctional groups fixed by means of a hydrocarbon group.

[0103] Organomodified silicones may be polydiaryl siloxanes, in particular polydiphenylsiloxanes, polydialkylsiloxanes and polyalkyl-arylsiloxanes functionalized by the organofunctional groups mentioned above.

[0104] Polyalkylarylsiloxanes are particularly chosen from among polydimethyl / methylphenylsiloxanes, linear and / or branched polydimethyl / diphenylsiloxanes with viscosities ranging from 1.105 to 5.102 m2 / s at 25°C.

[0105] Examples of these polyalkylarylsiloxanes include products marketed under the following names: - SILBIONE® oils from the 70 641 series by RHODIA; - the oils from the RHODORSIL® 70 633 and 763 series from RHODIA; - DOW CORNING 556 COSMETIC GRAD FLUID oil from DOW CORNING; - silicones from the PK series by BAYER such as the PK20 product; - BAYER's PN and PH series silicones, such as the PN1000 and PH1000 products - certain oils from the SF series of GENERAL ELECTRIC such as SF 1023, SF 1154, SF 1250, SF 1265.

[0106] Among organomodified silicones, we can also mention polyorganosiloxanes comprising: - substituted or unsubstituted amine groups such as the products marketed under the name GP 4 Silicone Fluid and GP 7100 by the company GENESEE. The substituted amine groups are in particular C1-C4 aminoalkyl groups; - alkoxylated groups, such as the product marketed under the name "SILICONE COPOLYMER F-755" by SWS SILICONES and ABIL WAX® 2428, 2434 and 2440 by the company GOLDSCHMIDT; - oxyalkylated groups, in particular oxyethylated groups, such as the product marketed under the name XIAMETER OFX-0193 FLUID by the company Dow Corning.

[0107] Volatile silicones are particularly chosen from those having a boiling point between 60°C and 260°C, and even more particularly from • Cyclic silicones containing 3 to 7 silicon atoms and preferably 4 to 6.

[0108] This includes, for example, octamethylcyclotetrasiloxane marketed in particular under the name "VOLATILE SILICONE 7207" by the company UNION CARBIDE or "SILBIONE 70045 V 2" by the company RHODIA, decamethylcyclopentasiloxane marketed under the name "VOLATILE SILICONE 7158" by the company UNION CARBIDE, "SILBIONE 70045 V 5" by the company RHODIA, as well as mixtures thereof.

[0109] We can also mention cyclocopolymers of the dimethylsiloxane / methylal-kylsiloxane type, such as "VOLATILE SILICONE FZ 3109" marketed by UNION CARBIDE, with the chemical structure: p D" - D'------D" - D' —। CH- 1 CH, rr with D” - O with d* • - If O — i I CH, CgH17

[0110] We can also mention mixtures of cyclic silicones with organic compounds derived from silicon, such as the mixture of octamethylcyclotetrasiloxane and tetratrimethylsilylpentaerythritol (50 / 50) and the mixture of octamethylcyclotetrasiloxane and oxy-l,r(hexa-2,2,2',2',3,3'-trimethylsilyloxy) bis-neopentane. • Linear volatile silicones having 2 to 9 silicon atoms and preferably possessing a viscosity less than or equal to 5 x 10⁶ m² / s at 25°C. Examples include hexamethyldisiloxane, octamethyltrisioloxane, and decamethyltetrasiloxane, marketed notably under the name Xiameter PMX200 by Dow Corning and "SH 200" by Toray Silicone. Silicones falling into this class are also described in the article published in Cosmetics and Toiletries, Vol. 91, Jan. 76, pp. 27-32 - TODD & BYERS "Volatile Silicone fluids for cosmetics". Preferably, linear volatile silicones contain 2 to 7 silicon atoms, better yet 3 to 6 silicon atoms.

[0111] Preferably, volatile silicones are chosen from cyclic silicones comprising 4 to 6 silicon atoms and linear silicones containing 2 to 9 silicon atoms.

[0112] Preferably, non-volatile silicones are chosen from polydialkyl-siloxanes, more particularly polydimethylsiloxanes, organomodified or non-organomodified.

[0113] More preferably, the composition according to the invention comprises one or more silicones selected from polydimethylsiloxanes; polydimethylsiloxanes modified by organofunctional groups selected from amine groups and oxyalkylated groups; and mixtures thereof.

[0114] According to a particular embodiment of the invention, the composition comprises one or more silicone(s) selected from polydimethylsiloxanes modified by one or more oxyalkylated groups.

[0115] According to another particular embodiment of the invention, the silicones are chosen from among the amino silicones.

[0116] Aminated silicone means any silicone comprising at least one primary, secondary, tertiary amine or one quaternary ammonium group.

[0117] The average molecular masses by weight of these amine-based silicones can be measured by Gel Permeation Chromatography (GPC) at room temperature (25°C) in polystyrene equivalents. The columns used are Styragel p-columns. The eluent is THF, and the flow rate is 1 ml / min. 200 µL of a 0.5% by weight silicone solution is injected into the THF. Detection is performed by refractometry and UV measurement.

[0118] Preferably, the amine-based silicone(s) that may be used in the context of the invention are chosen from:

[0119] a) polysiloxanes corresponding to formula (A): I 0H I —U si—o kw w I (THAT I NH | I | ] NH9 ] y'

[0120] in which x' and y' are integers such that the average molecular weight by weight (Mw) is between approximately 5,000 and 500,000;

[0121] b) Amino silicones conforming to formula (B):

[0122] R'aG3 a-Si(OSiG2)n-(OSiGbR'2 b)mO-SiG3 a-R'a (B)

[0123] in which:

[0124] - G, identical or different, designates a hydrogen atom, a phenyl group, OH, alkyl in CrC8, for example methyl, or alkoxy in CrC8, for example methoxy,

[0125] - a, same or different, denotes 0 or an integer from 1 to 3, in particular 0,

[0126] - b denotes 0 or 1, in particular 1,

[0127] - m and n are numbers such that the sum (n + m) varies from 1 to 2000, in particular from 50 to 150, where n can represent a number from 0 to 1999, and in particular from 49 to 149 and m can designate a number from 1 to 2000, and in particular from 1 to 10;

[0128] - R', identical or different, denotes a monovalent radical of formula -CqH2qL in where q is a number from 2 to 8, and L is an amine grouping, possibly quantized, chosen from the following groups:

[0129] -N(R")2; -N+(R")3 A-; -NR,'-QN(R,')2and-NR,'-Q-N+(R,')3 A-,

[0130] wherein R", identical or different, denotes hydrogen, phenyl, benzyl, or a monovalent saturated hydrocarbon radical, for example a C1-C20 alkyl radical; Q denotes a group of formula CrH2r, linear or branched, r being an integer from 2 to 6, preferably from 2 to 4; and A- represents a cosmetically acceptable anion, in particular a halide such as fluoride, chloride, bromide, or iodide.

[0131] Preferably, the amino silicones are chosen from the amino silicones of formula (B). Preferably, the amino silicones of formula (B) are chosen from the amino silicones corresponding to the following formulas (C), (D), (E), (F), and / or (G).

[0132] According to a first embodiment, the amino silicones corresponding to formula (B) are chosen from the silicones called "trimethylsilylamodi-methicone" corresponding to formula (C): "3 CH,. j GH. i <!-- (C ............ O— Ss------i------ |                              ! o- - j OS§(GI ch3 1 --1 H l / GH 7 G NH, m<br-->

[0133] in which m and n are numbers such that the sum (n + m) varies from 1 to 2000, in particular from 50 to 150, n being able to designate a number from 0 to 1999, and in particular from 49 to 149 and m being able to designate a number from 1 to 2000, and in particular from 1 to 10.

[0134] According to a second embodiment, the amino-based silicones corresponding to formula (B) are chosen from the silicones of the following formula (D): (0¾ NH?

[0135] in which:

[0136] - m and n are numbers such that the sum (n + m) varies from 1 to 1000, in particular from 50 to 250 and more particularly from 100 to 200; n can designate a number from 0 to 999 and in particular from 49 to 249 and more particularly from 125 to 175 and m can designate a number from 1 to 1000, in particular from 1 to 10, more particularly from 1 to 5;

[0137] - RI, R2, R3, whether identical or different, represent a hydroxy or alkoxy radical in C1-C4, at least one of the radicals RI to R3 designating an alkoxy radical.

[0138] Preferably the alkoxy radical is a methoxy radical.

[0139] The hydroxy / alkoxy molar ratio is preferably from 0.2:1 to 0.4:1 and preferably from 0.25:1 to 0.35:1 and more particularly is equal to 0.3:1.

[0140] The average molecular mass by weight (Mw) of these silicones preferably ranges from 2000 to 1,000,000, more particularly from 3500 to 200,000.

[0141] According to a third embodiment, the amino silicones corresponding to formula (B) are chosen from the following silicones of formula (E):

[0142] in which:

[0143] - p and q are numbers such that the sum (p+q) varies from 1 to 1000, in particular from 50 to 350, and more particularly from 150 to 250; p can designate a number from 0 to 999 and in particular from 49 to 349 and more particularly from 159 to 239 and q can designate a number from 1 to 1000, in particular from 1 to 10 and more particularly from 1 to 5;

[0144] - RI, R2, different, represent a hydroxy or alkoxy radical in C1-C4, one at minus the RI or R2 radicals designating an alkoxy radical.

[0145] Preferably the alkoxy radical is a methoxy radical.

[0146] The hydroxy / alkoxy molar ratio generally ranges from 1:0.8 to 1:1.1 and preferably from 1:0.9 to 1:1 and more particularly is equal to 1:0.95.

[0147] The average molecular mass by weight (Mw) of silicone is preferably from 2000 to 200000 and even more particularly from 5000 to 100000 and more particularly from 10000 to 50000.

[0148] Commercial products comprising structural silicones (D) or (E) may include in their composition one or more other amino silicones whose structure is different from formulas (D) or (E).

[0149] A product containing structure (D) amino silicones is offered by the company WACKER under the name BELSIL® ADM 652.

[0150] A product containing structure-amino silicones (E) is offered by WACKER under the name Fluid WR 1300®.

[0151] When these amino silicones are used, a particularly interesting embodiment is their use as an oil-in-water emulsion. The oil-in-water emulsion may comprise one or more surfactants. The surfactants may be of any type, but preferably cationic and / or nonionic. The average number size of the silicone particles in the emulsion generally ranges from 3 nm to 500 nanometers. Preferably, particularly as amino silicones of formula (E), microemulsions are used with an average particle size ranging from 5 nm to 60 nanometers (inclusive) and more particularly from 10 nm to 50 nanometers (inclusive). Thus, according to the invention, the amino silicone microemulsions of formula (E) offered under the names FINISH CT 96 E® or SLM 28020® by WACKER can be used.

[0152] According to a fourth embodiment, the amino silicones corresponding to formula (B) are chosen from the silicones of the following formula (F):

[0153] in which:

[0154] - m and n are numbers such that the sum (n + m) varies from 1 to 2000 and in by particular from 50 to 150, n can designate a number from 0 to 1999 and in particular from 49 to 149 and m can designate a number from 1 to 2000, and in particular from 1 to 10;

[0155] - A denotes a linear or branched alkylene radical having from 4 to 8 carbon atoms and preferably 4 carbon atoms. This radical is preferably linear.

[0156] The average molecular mass by weight (Mw) of these amino silicones preferably ranges from 2000 to 1000000 and even more particularly from 3500 to 200000.

[0157] A silicone meeting this formula is for example DOW CORNING's XIAMETER MEM 8299 EMULSION.

[0158] According to a fifth embodiment, the amino silicones corresponding to formula (B) are chosen from the silicones of the following formula (G):

[0159] in which:

[0160] - m and n are numbers such that the sum (n + m) varies from 1 to 2000 and in by particular from 50 to 150, n can designate a number from 0 to 1999 and in particular from 49 to 149 and m can designate a number from 1 to 2000, and in particular from 1 to 10;

[0161] - A denotes a linear or branched alkylene radical having from 4 to 8 carbon atoms and preferably 4 carbon atoms. This radical is preferably branched.

[0162] The average molecular mass by weight (Mw) of these amino silicones preferably ranges from 500 to 1,000,000 and even more particularly from 1,000 to 200,000.

[0163] A silicone meeting this formula is, for example, DOW CORNING's DC2-8566 Amino Fluid.

[0164] c) Amino silicones conforming to formula (H): .......Q ' rri (RkL—Si—0^4—Si—O 4—kàr-O-4—SUdlh J ï 1 ! 1 I L ] ( R, |

[0165] in which:

[0166] - R5 represents a monovalent hydrocarbon radical having from 1 to 18 atoms of carbon, and in particular an alkyl radical in Ci-Ci8, or alkenyl in C2-Ci8, for example methyl;

[0167] - R6 represents a divalent hydrocarbon radical, in particular an alkylene radical in CrCi8 or a divalent alkyleneoxy radical in CrCi8, for example in CrC8 linked to Si by a SiC bond;

[0168] - Q- is an anion such as a halide ion, in particular chloride or an acid salt organic, in particular acetate;

[0169] - r represents an average statistical value ranging from 2 to 20, in particular from 2 to 8;

[0170] - s represents an average statistical value ranging from 20 to 200, in particular from 20 to 50.

[0171] Such amino silicones are described in particular in US patent 4,185,087. - d) Quaternary ammonium silicones with the following formula:

[0172] in which:

[0173] - R7, identical or different, represent a monovalent hydrocarbon radical having from 1 to 18 carbon atoms, and in particular an alkyl radical in CrCi8, an alkenyl radical in C2-C[8 or a ring comprising 5 or 6 carbon atoms, for example methyl;

[0174] - R6 represents a divalent hydrocarbon radical, in particular an alkylene radical in CrCi8 or a divalent alkyleneoxy radical in CrCi8, for example in CrC8 linked to Si by a SiC bond;

[0175] - R8, identical or different, represent a hydrogen atom, a radical hy monovalent drocarbon having from 1 to 18 carbon atoms, and in particular an alkyl radical in Ci-Ci8, an alkenyl radical in C2-Ci8, a -R6-NHCOR7 radical;

[0176] - X- is an anion such as a halide ion, in particular chloride or an acid salt organic, in particular acetate;

[0177] - r represents an average statistical value ranging from 2 to 200, in particular from 5 to 100.

[0178] These silicones are described for example in application EP-A-0530974.

[0179] e) Amino silicones of formula (J): H^N - J - NH - (G^) ™ If “f”

[0180] in which:

[0181] - Ri, R2, R2 and R4, whether identical or different, denote a C1-C4 alkyl radical or a phenyl group,

[0182] - R5 designates a C1-C4 alkyl radical or a hydroxyl group,

[0183] - n is an integer ranging from 1 to 5,

[0184] - m is an integer ranging from 1 to 5, and

[0185] - x is chosen such that the amine index varies from 0.01 to 1 meq / g.

[0186] f) multiblock polyoxyalkylened amine silicones, of type (AB)n, A being a polysiloxane block and B being a polyoxyalkylened block comprising at least one amine group.

[0187] Said silicones are preferably made up of repeating units of formulas The following general terms apply:

[0188] [-(SiMe2O)xSiMe2 - R -N(R")- R'-O(C2H4O)a(C3H6O)b-R'-N(H)-R-]

[0189] or

[0190] [-(SiMe2O)xSiMe2 - R -N(R")- R' - O(C2H4O)a(C3H6O)b-]

[0191] in which:

[0192] - a is an integer greater than or equal to 1, preferably from 5 to 200, plus particularly ranging from 10 to 100;

[0193] - b is an integer between 0 and 200, preferably from 4 to 100, plus particularly between 5 and 30;

[0194] - x is an integer ranging from 1 to 10000, more particularly from 10 to 5000;

[0195] - R" is a hydrogen atom or a methyl;

[0196] - R, identical or different, represent a divalent hydrocarbon radical in C2-Ci2, linear or branched, possibly comprising one or more heteroatoms such as oxygen; preferably, R denotes an ethylene radical, a linear or branched propylene radical, a linear or branched butylene radical, or a -CH2CH2CH2OCH2 CH(OH)CH2- radical; preferably R denotes a -CH2CH2CH2OCH2CH(OH)CH 2- radical;

[0197] - R', identical or different, represent a divalent hydrocarbon radical in C2-Ci2 , linear or branched, possibly comprising one or more heteroatoms such as oxygen; preferably, R' denotes an ethylene radical, a linear or branched propylene radical, a linear or branched butylene radical, or a -CH2CH2CH2OCH2 CH(OH)CH2- radical; preferably R' denotes -CH(CH3)-CH2-.

[0198] The siloxane blocks preferably represent 50 and 95% by moles of the total weight of the silicone, more particularly 70 to 85% by moles.

[0199] The amine content is preferably between 0.02 and 0.5 meq / g of copolymer in a 30% solution in dipropylene glycol, more particularly between 0.05 and 0.2.

[0200] The average molecular mass by weight (Mw) of silicone is preferably between 5000 and 1000000, more particularly between 10000 and 200000.

[0201] We can notably cite silicones marketed under the names Silsoft A-843 or Silsoft A+ by Momentive.

[0202] g) and mixtures thereof.

[0203] According to a particular embodiment of the invention, the composition contained in the device according to the invention further comprises at least one volatile silicone.

[0204] More preferably according to this embodiment, the composition contained in the device according to the invention further comprises at least one linear volatile silicone having 2 to 9 silicon atoms (in particular 2 to 4 silicon atoms).

[0205] Even better according to this embodiment, the composition contained in the device according to the invention further comprises at least one silicone selected from hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, and mixtures thereof; and more specifically, silicone is hexamethyldisiloxane (INCI name: disiloxane).

[0206] Preferably, when the composition contained in the device according to the invention includes at least one silicone, the total silicone content is between 0.1 and 30% by weight, more preferably between 1 and 20% by weight, more preferably still between 5 and 15% by weight, relative to the total weight of said composition.

[0207] Preferably, when the composition contained in the device according to the invention includes at least one volatile silicone, the total silicone content is between 0.1 and 30% by weight, more preferably between 1 and 20% by weight, more preferably still between 5 and 15% by weight, relative to the total weight of said composition.

[0208] Preferably, the dynamic viscosity of the composition contained in the device according to the invention at a temperature of 25°C and at atmospheric pressure is in the range of 0.5 to 50 mPa.s; more preferably from 1 to 25 mPa.s; more preferably still from 2 to 10 mPa.s.

[0209] The dynamic viscosity of the compositions according to the invention can be measured using a rheometer such as a Rheomat RM180, at 25°C and at a rotation speed of 200 rpm, the measurement being carried out after 30 s of rotation.

[0210] The device according to the invention is devoid of a propellant agent.

[0211] Similarly, the composition contained in the device according to the invention is devoid of a propellant agent.

[0212] For the purposes of this invention, "propellant" means a propellant other than air.

[0213] By the expression "devoid of propellant" it is understood that the composition contained in the device according to the invention does not include a propellant, or that the propellant(s) present in said composition are included in a total content less than or equal to 1% by weight, preferably less than or equal to 0.5% by weight, more preferably less than or equal to 0.1% by weight, better less than or equal to 0.05% by weight, relative to the total weight of said composition, and even better free of propellant (0% by weight).

[0214] As propellants or gases, the following may be mentioned in particular: volatile hydrocarbons, possibly halogenated (for example chlorinated and / or fluorinated); dimethyl ether; and mixtures thereof; in particular dimethyl ether, C3-C5 alkanes, trichlorofluoromethane, dichlorodifluoromethane, chlorodifluoromethane, 1,1,1,2-tetrafluoroethane, chloropentafluoroethane, l-chloro-l,l-difluoroethane, 1,1-difluoroethane, 1,3,3,3-tetrafluoropropene, and mixtures thereof; and more particularly C3-C5 alkanes, such as propane, isopropane, n-butane, isobutane, pentane, and mixtures thereof.

[0215] The composition contained in the device according to the invention may optionally include further one or more additives, such as thickeners or viscosity regulators, natural or synthetic, other than the fixing polymers described above; vitamins or provitamins; polymers other than the fixing polymers described above; surfactants; preservatives; colorants; perfumes.

[0216] A person skilled in the art shall take care to choose any additives and their quantity so that they do not impair the properties of the composition contained in the device according to the invention.

[0217] These additives are generally present in the composition in an amount ranging from 0 to 20% by weight relative to the total weight of the composition.

[0218] The composition according to the invention is preferably cosmetic, and more particularly a lacquer for styling keratin fibers, i.e. for shaping and / or fixing keratin fibers. the device according to the invention

[0219] The invention relates to an aerosol device comprising the composition as described above, a container containing said composition, and at least one mechanical spraying system for said composition.

[0220] The container holding the pressurized composition may be opaque or transparent. It may be made of glass, polymer material or metal, and optionally coated with a protective varnish layer.

[0221] The mechanical spraying system for said composition is generally made up of a distribution valve controlled by a distribution head, itself comprising a nozzle through which the composition is sprayed.

[0222] The device according to the invention makes it possible to spray the composition, in the form of an aerosol (continuous spray), and this without the aid of a propellant agent.

[0223] More preferably, the mechanical spraying system further comprises at least one pumping means, advantageously configured to increase the pressure inside said container.

[0224] When the mechanical spraying system includes said pumping means, the user can operate the pumping means one or more times (for example, approximately 10 pump strokes) to increase the pressure by adding air inside said container. The overpressure thus generated inside the container allows, when the spraying system of the device according to the invention is operated, the composition to be sprayed in aerosol form (continuous spray) outside the device, without the aid of a propellant.

[0225] Preferably, the pressure inside said container can go up to 5x105 Pa, more preferably up to 4x105 Pa, and more preferably still up to 3x105 Pa.

[0226] Preferably, the relative operating pressure of the device according to the invention is between 1 x O5 and 4 x O5 Pa; more preferably between 2 x O5 and 3 x O5 Pa.

[0227] Several devices including this type of mechanical spraying system and pumping means are described in particular in applications WO 94 / 07770, US 6 193 115, US 6 170 716 and WO 93 / 16809.

[0228] The aerosol device according to the invention does not spray said composition in the form of foam.

[0229] The device according to the invention preferably sprays the composition in fine droplets (in the form of a continuous spray).

[0230] Preferably, the average volume size of the sprayed composition droplets is in the range of 1 to 200 µm; more preferably from 10 to 100 µm; more preferably still from 20 to 50 µm.

[0231] The average volume size of the sprayed droplets of the composition according to the invention can be measured using the known method of dynamic light scattering (DLS). A suitable device for this determination is the Malvem Spraytec particle size analyzer (laser / spray distance = 20 cm; measurement frequency = 5 Hz).

[0232] The invention also relates to a method for treating keratin fibers comprising at least one step of spraying said keratin fibers with a composition as described above, using an aerosol device without a propellant agent.

[0233] Preferably, the treatment process according to the invention is a styling process, i.e. shaping and / or fixing, of keratin fibers.

[0234] Preferably, the composition is sprayed onto the keratin fibers by means of a device according to the invention comprising a container containing said composition and a mechanical spraying system for said composition further comprising more preferably a pumping means advantageously configured to increase the pressure inside said container.

[0235] Preferably, the composition is sprayed in the form of droplets.

[0236] In a first embodiment of the process according to the invention, the composition is applied to wet hair.

[0237] In a second embodiment of the process according to the invention, the composition is applied to dry hair.

[0238] Preferably, the application of the composition to the keratin fibers is not followed by rinsing.

[0239] Advantageously, the keratin fibers are not rinsed with water, at least two hours, more preferably at least three hours, more preferably still at least four hours, after the spraying step of the process according to the invention.

[0240] The following examples serve to illustrate the invention without, however, being limiting in nature. Examples:

[0241] The compositions Al, A2, A3, A4, A5, A6 and A7 according to the invention were prepared from the ingredients indicated in the table below, the quantities of which are expressed as % by weight of active material (AM).

[0242] [Tables 1] Ingrédients Al A2 A3 Poloxamer 184 0,70 0,70 0,70 Acry late s / t-B uty lacry lamide Copolymer 7 - - VP / VA copolymer - 7 - VA / Crotonates / Vinyl neo-decanoate copolymer - - 7 Disiloxane - - 10 Aminométhyl propanol 0,86 - 0,73 Parfum Qs Qs Qs Ethanol Qsp 100 Qsp 100 Qsp 100

[0243] [Tableaux2] Ingrédients A4 A5 Poloxamer 184 0,70 - Poloxamer 182 - 0,70 VA / Crotonates / Vinyl neo-decanoate copolymer 7 7 Aminométhyl propanol 0,73 0,73 Parfum Qs Qs Ethanol Qsp 100 Qsp 100

[0244] [Tableaux3] Ingrédients A6 A7 Poloxamer 184 1 1 Disiloxane - 10 VA / Crotonates / Vinyl neo-decanoate copolymer 7 7 Aminométhyl propanol 0,73 0,73 Parfum Qs Qs Ethanol Qsp 100 Qsp 100

[0245] The compositions Al to A7 according to the invention were each packaged in separate devices according to the invention, each having a spray nozzle with a diameter of 0.33 mm. After 10 pump strokes, the pressure inside the container is 2 x 10⁵ Pa (2 bar). These devices do not contain a propellant.

[0246] The average volume sizes of the droplets of compositions A6 and A7 according to the invention, sprayed by the device according to the invention, were measured according to the known method of dynamic light scattering (DLS) using a Malvem Spraytec granulometer (laser / spray distance=20cm; measurement frequency=5Hz).

[0247] The average volume sizes of the droplets of compositions A6 and A7 according to the invention, sprayed by the device according to the invention, measured are respectively 38pm and 37pm.

[0248] It was observed that the quality of the spray obtained with each of the devices according to the invention was good, in particular: a continuous homogeneous and regular spray, fine droplets, and the absence of nozzle clogging.

[0249] Each of the compositions Al to A7 according to the invention was also sprayed onto a separate strand of hair.

[0250] It has been observed that the compositions Al to A7 according to the invention provide good fixation and good hold of the hair.

[0251] In addition, it has been observed that the compositions Al to A7 according to the invention provide a natural appearance to the hairstyle and a particularly soft and pleasant feel to the hair, and allow for fluid movement of the hair.

Claims

Demands

1. Aerosol device, without a propellant agent, comprising: i. a composition comprising: a. 0.5% to 5% by weight, relative to the total weight of the composition, of one or more polycondensates of ethylene oxide and propylene oxide of formula (A): H-(O-CH2-CH2)a-(O-CH(CH3)-CH2)b-(O-CH2-CH2)a. -OH (A) in which: a and a', identical or different, are integers between 2 and 150, and b is an integer between 1 and 100, b. 1% to 15% by weight, relative to the total weight of the composition, of one or more anionic fixing polymer(s) with carboxylic groups, and c. one or more solvents chosen from water, organic solvents, and mixtures thereof; ii. a container containing said composition; and iii. at least one mechanical spraying system for said composition.

2. Device according to the preceding claim, characterized in that the polycondensate(s) of ethylene oxide and propylene oxide are selected from Poloxamer 108, Poloxamer 338, Poloxamer 124, Poloxamer 122, Poloxamer 407, Poloxamer 184, Poloxamer 238, Poloxamer 237, Poloxamer 188, and mixtures thereof; more preferably the polycondensate of ethylene oxide and propylene oxide is Poloxamer 184.

3. Device according to any one of the preceding claims, characterized in that the content of ethylene oxide and propylene oxide polycondensate(s) in the composition is in the range of 0.75% to 3% by weight, relative to the total weight of said composition.

4. A device according to any one of the preceding claims, characterized in that the anionic fixing polymer(s) with groups carboxylics are chosen from crotonic acid copolymers; preferably from Vinyl Acetate / Crotonates / Vinyl Neodecanoate copolymers, Vinyl Acetate / Crotonates / Vinyl Decanoate copolymers, Vinyl Acetate / Crotonates copolymers, Vinyl Acetate / Vinyl Butyl Benzoate / Crotonates copolymers, and mixtures thereof; and even better the fixing polymer is a Vinyl Acetate / Crotonates / Vinyl Neodecanoate copolymer.

5. Device according to any one of the preceding claims, characterized in that the content of fixing polymer(s) in the composition is in the range of 2% to 10% by weight, and even better of 3% to 8% by weight, relative to the total weight of said composition.

6. Device according to any one of the preceding claims, characterized in that the solvent(s) are chosen from organic solvents, preferably chosen from C2-C8 alcohols; more preferably from C2-C6 monoalcohols; more preferably still from C2-C4 monoalcohols; even better the solvent is ethanol.

7. Device according to any one of the preceding claims, characterized in that the content of organic solvent(s) in the composition is in the range of 10 to 99% by weight, preferably 30 to 98% by weight, more preferably 50 to 97% by weight, and more preferably 70 to 95% by weight, relative to the total weight of said composition.

8. A device according to any one of the preceding claims, characterized in that the composition further comprises at least one silicone; preferably at least one volatile silicone; more preferably at least one linear volatile silicone having 2 to 9 silicon atoms; more preferably still at least one silicone selected from hexamethyldisiloxane, octamethyltrisiloxane, decamethylte-trasiloxane, and mixtures thereof; and even better the silicone is hexamethyldisiloxane.

9. Device according to the preceding claim, characterized in that the silicone content(s) in the composition is in the range of 0.1 to 30% by weight, preferably 1 to 20% by weight, and more preferably 5 to 15% by weight, relative to the total weight of said composition.

10. Device according to any one of the preceding claims, ca- characterized in that the dynamic viscosity of the composition, at a temperature of 25°C and at atmospheric pressure, is in the range of 0.5 to 50 mPa.s; preferably from 1 to 25 mPa.s; more preferably from 2 to 10 mPa.s.

11. Device according to any one of the preceding claims, characterized in that the mechanical spraying system of said composition comprises at least one pumping means.

12. Use of an aerosol device as defined in any one of claims 1 to 11, for the treatment, preferably the capping, of keratin fibers.

13. A method for treating, preferably for styling, keratin fibers, comprising at least one step of spraying said keratin fibers with a composition as defined in any one of claims 1 to 10, using an aerosol device without a propellant agent.

14. Processing method according to the preceding claim, characterized in that said composition is sprayed in the form of droplets.