 PROCESS FOR THE COSMETIC TREATMENT OF KERATIN FIBERS COMPRISING THE APPLICATION OF A BASIC COMPOSITI
专利摘要:
The present invention relates to a process for the cosmetic treatment of keratinous fibers, preferably human keratinous fibers such as the hair, in particular for the conditioning of keratinous fibers, using a combination of at least two distinct compositions, the first composition comprising one or more several oxyalkylenated silicones, preferably oxyethylenated silicones and one or more first cationic surfactants and the second composition comprising water and one or more second cationic surfactants. The invention also relates to a kit comprising both compositions. Finally, the invention relates to a cosmetic composition for the treatment of keratinous fibers ready to be used. 公开号:FR3064476A1 申请号:FR1752806 申请日:2017-03-31 公开日:2018-10-05 发明作者:Anne-Sophie BRAC DE LA PERRIERE；Sandrine Maggio 申请人:LOreal SA； IPC主号:
专利说明:
© Publication number: 3,064,476 (to be used only for reproduction orders) ©) National registration number: 17 52806 ® FRENCH REPUBLIC NATIONAL INSTITUTE OF INDUSTRIAL PROPERTY COURBEVOIE ©) Int Cl 8 : A 61 K8 / 891 (2017.01), A 61 Q 5/00 A1 PATENT APPLICATION ©) Date of filing: 03.31.17. ©) Applicant (s): L'OREAL Société anonyme— FR. ©) Priority: (72) Inventor (s): BRAC DE LA PERRIERE ANNE- SOPHIE and MAGGIO SANDRINE. (43) Date of public availability of the request: 05.10.18 Bulletin 18/40. ©) List of documents cited in the report preliminary research: Refer to end of present booklet @) References to other national documents ©) Holder (s): L'OREAL Société anonyme. related: ©) Extension request (s): @) Agent (s): CASALONGA AXEL. PROCESS FOR THE COSMETIC TREATMENT OF KERATINIC FIBERS COMPRISING THE APPLICATION OF A BASIC COMPOSITION AND A COMPOSITION COMPRISING A CATIONIC SURFACTANT. FR 3,064,476 - A1 (3y / The present invention relates to a cosmetic treatment process for keratin fibers, preferably human keratin fibers such as the hair, in particular for conditioning keratin fibers, using a combination of at least two separate compositions, the first composition comprising one or more oxyalkylenated, preferably oxyethylenated silicones and one or more first cationic surfactants and the second composition comprising water and one or more second cationic surfactants. The invention also relates to a kit comprising the two compositions. Finally, the invention relates to a cosmetic composition for the treatment of keratin fibers ready for use. i Cosmetic treatment method for keratin fibers comprising the application of a base composition and of a composition comprising a cationic surfactant The present invention relates to a cosmetic treatment process for keratin fibers, preferably human keratin fibers such as the hair, in particular for conditioning keratin fibers, using a combination of at least two separate compositions. The invention also relates to a kit comprising the two compositions. Finally, the invention relates to a cosmetic composition for the treatment of keratin fibers ready for use. The hair is generally damaged and weakened by the action of external atmospheric agents such as light and bad weather, and by mechanical or chemical treatments such as brushing, combing, dyeing, bleaching, perms and / or hair straighteners. Thus, to remedy these drawbacks, it is now customary to use hair care implying the use of care compositions which make it possible to condition the hair following these treatments in order to give them in particular shine, softness, suppleness, lightness, a natural touch as well as disentangling properties. These hair care compositions may for example be conditioning shampoos or compositions to be applied before or after the shampoos, and which may be in the form of gels, hair lotions or more or less thick creams. More and more consumers are looking for personalized care prepared just at the time of application to specifically meet their needs, especially when they go to a hairdressing professional. Thus, the use of separate compositions, one serving as a common base for all consumers, and the other comprising the ingredients intended to provide targeted packaging performance can be advantageous. The desired packaging performance, which can be more or less marked depending on the consumer, include an improved surface condition, ease of disentangling, smooth feel, coating, improved hair resistance, and shine. . It is also attractive for the consumer to witness the formation of a texture mixture of the cream or care mask type from compositions with a totally different appearance, for example from fluid liquid compositions, by simple mixing with using a spatula. Mixing at the time of use can also allow the joint use of ingredients which would be incompatible together in a conventional composition. Thus, the objective of the invention is to propose modular care compositions prepared just before application to the hair from at least one basic composition common to all the uses and another composition chosen from a panel of according to the specific needs of the consumer's hair. The subject of the invention is therefore a method of cosmetic treatment of keratin fibers, preferably human keratin fibers such as the hair, comprising: (i) a mixing step of at least: a first composition comprising one or more oxyalkylenated, preferably oxyethylenated, silicones and one or more first cationic surfactants, and - A second composition comprising water and one or more second cationic surfactants, so as to obtain a final cosmetic composition, then (ii) a step of applying the final cosmetic composition to the keratin fibers. Thus, the method according to the invention makes it possible to provide cosmetics to the treated hair, in particular an improved surface condition, an ease of disentangling, a smooth feel, of the coating, an improved resistance of the hair, and of shine. In addition, the preparation of the final cosmetic composition in the process according to the invention is easy, by simple mixing of at least two separate compositions. In addition, the final composition is easily and quickly rinsed off. Another object of the present invention is a kit comprising at least two compartments: a first compartment comprising a first composition as defined above, - a second compartment comprising a second composition as defined above. Finally, an object of the present invention relates to a cosmetic composition for the cosmetic treatment of keratin fibers comprising: i) one or more non-amino oxyalkylenated silicones, preferably non-amino oxyethylenated silicones, ii) one or more first cationic surfactants, iii) one or more second cationic surfactants different from the cationic surfactants (ii), iv) of water. This cosmetic composition advantageously corresponds to the final cosmetic composition obtained at the end of the mixing step of the process according to the invention. The final composition is generally in the form of a cream, has a pleasant texture, and is easy to apply and spread over the keratin fibers. Other objects, characteristics, aspects and advantages of the invention will appear even more clearly on reading the description and the examples which follow. In what follows, and unless otherwise indicated, the limits of a domain of values are included in this domain, in particular in the expressions "included between" and "going from ... to ...". Furthermore, the expressions “at least one” and “at least” used in the present description are respectively equivalent to the expressions “one or more” and “greater than or equal”. By “keratin fibers” according to the present application, we mainly designate human keratin fibers, and in particular the hair. As explained above, the method according to the invention comprises a step of mixing at least: a first composition comprising one or more oxyalkylenated silicones and one or more first cationic surfactants, and - a second composition comprising water and one or more second cationic surfactants, so as to obtain a final cosmetic composition. Preferably, the first composition is anhydrous. By “anhydrous composition” within the meaning of the present invention, it is meant that this composition comprises less than 10% by weight, and preferably less than 9% by weight of water relative to the total weight of the composition. Preferably, the oxyalkylenated silicone (s) of the first composition are oxyethylenated. Advantageously, the oxyalkylenated silicone (s) of the first composition are chosen from non-amino oxyalkylenated silicones, better still from non-amino oxyethylenated silicones. By “non-amino” silicones, it is understood within the meaning of the present invention that these silicones do not include in their amine functional structure, whether they are in the form of primary, secondary, tertiary amine or in the form of a group. quaternary ammonium. According to the invention, the term “oxyalkylenated silicone” denotes any silicone comprising at least one oxyalkylenated group of type (-C x H2 X O) a in which x can vary from 2 to 6 and a is greater than or equal to 1, preferably greater or equal to 2. In accordance with the invention, the oxyalkylenated silicones are preferably chosen from the compounds of general formulas (I), (II), (III) or (IV) below: p - ch 3 - -CH 3 - Γ Î H3 _ ch 3 If —0— Yes "Ii n qî n I- Si-R U ch 3 L Ri 0 -r 2 m L ch 3 J n CH 3 Ç H 3 - ÇH 3 - -H 3 - R 1 - SÎ-O If n if n ch 3 L r 2 J P Lqh 3 J Ç H 3 - ÇH 3 - -H 3 - R 2 - Si-0 If n if n ch 3 L Ri J 0 Lqh 3 R 3-Si Hh 3 O — Si-I - x ch 3 (I) Hh 3 If - ch 3 R 1 (Π) ch 3 Si— R 2 ch 3 (III) (OC 2 H 4 ) a (OC 3 H 6 ) b OR (IV) formulas (I), (II), (III) and (IV) in which: - Ri, identical or different, represents an alkyl radical, linear or branched, C1-C30 or phenyl, - R2, identical or different, represents a radical -CcH 2c -O (C2H 4 O) a (C 3 H 6 O) b -R 5 or a radical -C c H 2 cO- (C 4 H 8 O) a -R 5 , - R3 and R 4 , identical or different, denote an alkyl radical, linear or branched, Ci to C12, and preferably the methyl radical, - R5, identical or different, is chosen from a hydrogen atom, an alkyl radical, linear or branched, from 1 to 12 carbon atoms, an alkoxy radical, linear or branched, from 1 to 6 carbon atoms, a radical acyl, linear or branched, from 2 to 30 carbon atoms, a hydroxyl radical, -SO3M, Ci-C6 aminoalkoxy optionally substituted on the amine, C2-C6 aminoacyl optionally substituted on the amine, -NHCH2CH2COOM, -N (CH2CH 2 COOM) 2, aminoalkyl optionally substituted on the amine and on the alkyl chain, carboxyacyl in C2-C30, a group optionally substituted by one or two substituted aminoalkyl radicals, -CO (CH 2 ) d COOM, -COCHR 7 (CH 2 ) d COOM, -NHCO (CH 2 ) dOH, -NH3Y, a phosphate group, - M, identical or different, denotes a hydrogen atom, Na, K, Li, NH 4 or an organic amine, - R7 denotes a hydrogen atom or an SO3M radical, - d varies from 1 to 10, - m varies from 0 to 20, - n varies from 0 to 500, - o varies from 0 to 20, - p varies from 1 to 50, - a varies from 0 to 50, - b varies from 0 to 50, - a + b is greater than or equal to 2, - c varies from 0 to 4, - x varies from 1 to 100, - Y represents a monovalent inorganic or organic anion such as halide (chloride, bromide), sulfate, carboxylate (acetate, lactate, citrate), provided that when the silicone is of formula (II) with R5 denoting hydrogen then n is greater than 12. Such silicones are for example marketed by the company GOLDSCHMIDT under the trade names ABIL WE 09, ABIL EM 90, ABIL B8852, ABIL B8851, ABIL B8843, ABIL B8842, by the company DOW CORNING under the names FLUID DC 190, DC 3225 C , Q2-5220, Q25354, Q2-5200, by the company RHONE POULENC under the names SILBIONE HUILE 70646, RHODORSIL HUILE 10634, by the company GENERAL ELECTRIC under the names SF1066, SF1188, by the company SWS SILICONES under the name SILICONE COPOLYMER F 754, by the company AMERCHOL under the name SILSOFT BEAUTY AID SL, by the company SHIN-ETSU under the name KF 351, by the company WACKER under the name BELSIL DMC 6038, by the company SILTECH under the names SILWAX WD-C, SILWAX WD-B, SILWAX WD-IS, SILWAX WSL, SILWAX DCA 100, SILTECH AMINE 65, by the company FANNING CORPORATION under the names FANCORSIL SLA, FANCORSIL LIM1, by the company PHOENIX under the name PECOSIL. These silicones are in particular described in patents US-A-5,070,171, US-A-5,149,765, US-A-5,093,452 and US-A-5,091,493. Preferably, the oxyalkylenated silicones corresponding to the general formulas (II) or (III) are used. More particularly, these formulas meet at least one of, and preferably all, of the following conditions: - c is equal to 2 or 3, - Ri denotes the methyl radical, - R5 represents a hydrogen atom, a methyl radical, a C12-C22 acyl radical, - a varies from 2 to 25 and more particularly from 2 to 20, - b is equal to 0, - n varies from 0 to 100, - p varies from 1 to 20. Even more preferably, the oxyalkylenated silicone (s) according to the invention are chosen from non-amino oxyethylenated silicones, preferably of formula (II) in which: - R2, identical or different, represents a radical -CcH 2c -O (C2H 4 O) a (C 3 H 6 O) b -R 5 , - c is equal to 2 or 3, - Ri denotes the methyl radical, - R5 represents a hydrogen atom, - a varies from 2 to 25 and more particularly from 2 to 20, - b is equal to 0, - n varies from 0 to 100, - p varies from 1 to 20. The oxyalkylenated silicones according to the invention can also be chosen from the silicones of formula (V) below: ([Z (R 2 SiO) q R ' 2 SiZO] [(C „H 2 „ O) r ]) s (V) formula (V) in which: - R2 and R'2, identical or different, represent a monovalent hydrocarbon radical, - n is an integer ranging from 2 to 4, q is a number greater than or equal to 4, preferably between 4 and 200 and even more particularly between 4 and 100, r is a number greater than or equal to 4, preferably between 4 and 200 and even more particularly between 5 and 100, - s is a number greater than or equal to 4, preferably between 4 and 1000 and even more particularly between 5 and 300, Z represents a divalent organic group which is linked to the adjacent silicon atom by a carbon-silicon bond and to a polyoxyalkylene block by an oxygen atom, the average molecular weight of each siloxane block is between approximately 400 and approximately 10,000, that of each polyoxyalkylene block being between approximately 300 and approximately 10,000, the siloxane blocks represent from about 10% to about 95% by weight of the block copolymer, - The number average molecular weight of the block copolymer varies from 2,500 to 1,000,000 and preferably between 3,000 and 200,000 and even more particularly between 6,000 and 100,000. R 2 and R ′ 2 are preferably chosen from the group comprising linear or branched alkyl radicals, such as, for example, methyl, ethyl, propyl, butyl, pentyl, hexyl, octyl, decyl, dodecyl, aryl radicals, for example phenyl, naphthyl, aralkyl or alkylaryl radicals such as, for example, benzyl, phenylethyl, tolyl, xylyl radicals. Z is preferably -R-, -R-CO-, -R-NHCO-, -R-NH-CONH-R'-, -R-OCONH-R'-NHCO-, where R is a divalent alkylene group, linear or branched in C 1 -C 6, such as for example ethylene, propylene or butylene, linear or branched and R ′ is a divalent alkylene group or a divalent arylene group such as -C6H 4 -, -CôLUC 6 H 4 -, -C 6 H 4 -CH 2 -C 6 H 4 -, -C 6 H 4 -C (CH3) 2 C 6 H 4 -. Even more preferably, Z represents a divalent alkylene radical, more particularly the radical -C3H6- or the radical -C 4 H 8 -, linear or branched. The preparation of the block copolymers used in the context of the present invention is described in European application EP 0 492 657 A1, the teaching of which is included in the present description. Such products are for example marketed under the name SILICONE FLUID FZ-2172 by the company OSI. Preferably, the oxyalkylenated silicone (s) of the first composition represent from 0.01 to 10% by weight, preferably from 0.05 to 5% by weight, and more preferably from 0.1 to 2% by weight, per relative to the total weight of the first composition. As described above, the first composition and the second composition which can be used in the process according to the invention also comprise one or more cationic surfactants, preferably non-silicone. ίο The term “cationic surfactant” means a positively charged surfactant when it is contained in a composition which can be used according to the invention. This surfactant can carry one or more positive permanent charges or contain one or more cationizable functions within a composition which can be used according to the invention. The first cationic surfactant (s) of the first composition and the second cationic surfactant (s) of the second composition are preferably chosen, independently of one another, from primary, secondary or tertiary fatty amines, optionally polyoxyalkylenated, or their salts, quaternary ammonium salts, and mixtures thereof. The fatty amines generally comprise at least one C8-C30 hydrocarbon chain Mention may in particular be made, as quaternary ammonium salts, for example: - those corresponding to the following general formula (VI): R 8 / R 10 NX R 9 R n (VI) Formula (VI) in which: the groups Rg to Ru, which may be identical or different, represent an aliphatic group, linear or branched, comprising from 1 to 30 carbon atoms, or an aromatic group such as aryl or alkylaryl, at least one of the groups Rg to Ru denoting an aliphatic radical, linear or branched, comprising from 8 to 30 carbon atoms, preferably from 12 to 24 carbon atoms. The aliphatic groups can comprise heteroatoms such as in particular oxygen, nitrogen, sulfur and halogens. The aliphatic groups are for example chosen from C1-C30 alkyl, C1-C30 alkoxy, polyoxyalkylenated (C2-C6), C1-C30 alkylamide, alkyl (Ci 2 3064476 C22) amidoalkyl (C2-C6), alkyl (Ci2-C 22) acetate, and hydroxyalkyl in X 'is an anion chosen from the group of halides, phosphates, acetates, lactates, (Ci-C4) alkyl sulfates, (Ci-C4) alkyl - or (Ci-C4) alkyl aryl-sulfonates. Among the quaternary ammonium salts of formula (VI), tetraalkylammonium salts are preferred on the one hand, such as, for example, the dialkyldimethylammonium or alkyltrimethylammonium salts in which the alkyl group contains approximately from 12 to 22 atoms of carbon, in particular the behenyltrimethylammonium salts, distearyldimethylammonium, cetyltrimethylammonium, benzyldimethylstearylammonium or, on the other hand, the palmitylamidopropyltrimethyl ammonium salts, stearamidopropyltrimethylammonium, stearamidylethylammethyl stearyl dimethylammonium acetylammethyl ester ammonium salts marketed under the name CERAPHYL® 70 by the company VAN DYK. It is particularly preferred to use the chloride salts of its compounds. - the quaternary ammonium salts of imidazoline, such as for example those of formula (VII) below: R. (VII) Formula (VII) in which: R12 represents an alkenyl or alkyl group comprising from 8 to 30 carbon atoms, for example derived from tallow fatty acids, R13 represents a hydrogen atom, a C1-C4 alkyl group or an alkenyl or alkyl group having from 8 to 30 carbon atoms. 2+ 2X Ri4 represents a C1-C4 alkyl group, Ris represents a hydrogen atom, an alkyl group CiC 4, X 'is an anion chosen from the group of halides, phosphates, acetates, lactates, alkylsulphates, alkyl- or alkylarylsulfonates, the alkyl and aryl groups of which preferably comprise from 1 to 20 carbon atoms and from 6 to 30 carbon atoms respectively. Preferably, R12 and R13 denote a mixture of alkenyl or alkyl groups containing from 12 to 21 carbon atoms, for example derived from tallow fatty acids, Ri 4 denotes a methyl group, R15 denotes a hydrogen atom. Such a product is for example marketed under the name REWOQUAT® W 75 by the company REWO; - the quaternary di- or tri-ammonium salts of formula (VIII): R 17 ^ 19 R 16 — N— (CH 2 ) 3 - N— R 21 R R j8 20 (VIII) Formula (VIII) in which: - Ri6 denotes an alkyl group comprising approximately from 16 to 30 carbon atoms optionally hydroxylated and / or optionally interrupted by one or more oxygen atoms, - R17 denotes hydrogen, an alkyl group containing from 1 to 4 carbon atoms or a group - (CH 2 ) 3-N + (Ri6a) (Ri7a) (Ri8a), Ri6a, Ri7a, Risa, identical or different denoting hydrogen or an alkyl group containing from 1 to 4 carbon atoms, Ris, R19, R20 and R21, identical or different, denote hydrogen or an alkyl group containing from 1 to 4 carbon atoms, and - X 'is an anion chosen in particular from the group of halides, acetates, phosphates, nitrates, (Ci-C4) alkyl sulfates, (Ci-C4) alkyl sulfonates and (Ci-C4) alkyl aryl-sulfonates, in particular methylsulfate and ethyl sulfate. Such compounds are, for example, Finquat CT-P (Quaternium 89) and Finquat CT (Quaternium 75) offered by the company FINETEX. - quaternary ammonium salts containing one or more ester functions of formula (IX) below: o (Ç s h 2s 0) z —r 25 r 2 — C - (- OC ^ r2 (OH) r7 ^ —N ^ - (- C t H t2 (OH) ,, —O- ^ R 23 χ ~ Formula (IX) in which: - R22 is chosen from C 1 -C 6 alkyl groups and C 1 -C 6 hydroxyalkyl or dihydroxyalkyl groups, - R23 is chosen from the group R26-C (= O) -; linear or branched, saturated or unsaturated C1 to C22 hydrocarbon R27 groups; and the hydrogen atom, - R25 is chosen from the group R28-C (= O) -; linear or branched, saturated or unsaturated C1-C6 hydrocarbon groups R29; and the hydrogen atom, - R24, R26 and R28, identical or different, are chosen from C7-C21 hydrocarbon groups, linear or branched, saturated or unsaturated, - r, s and t, identical or different, are integers ranging from 2 to 6, - rl and tl, identical or different, are worth 0 or 1, - r2 and t2, identical or different, are integers such that r2 + rl = 2r and tl + t2 = 2t, - y is an integer from 1 to 10, - x and z, identical or different, are integers ranging from 0 to 10, it being understood that the sum x + y + z is worth from 1 to 15, - X 'is an anion, provided that when x = 0 then R 2 3 denotes R 27 and that when z = 0 then R 2 5 denotes R 2 9. The alkyl groups R 22 can be linear or branched, preferably linear. Preferably, R 22 denotes a methyl, ethyl, hydroxyethyl or dihydroxypropyl group, and more particularly a methyl or ethyl group. Advantageously, the sum x + y + z is worth from 1 to 10. When R 2 3 is a hydrocarbon R 27 group, it can comprise from 12 to 22 carbon atoms, or even comprise from 1 to 3 carbon atoms. When R 2 5 is a hydrocarbon R 2 9 group, it preferably has 1 to 3 carbon atoms. Advantageously, R 24 , R 2 6 and R 28 , identical or different, are chosen from C11-C21 hydrocarbon groups, linear or branched, saturated or unsaturated, and more particularly from C11-C21 alkyl and alkenyl groups, linear or branched. Preferably, x and z, identical or different, are worth 0 or 1. Advantageously, y is equal to 1. Preferably, r, s and t, identical or different, are worth 2 or 3, and even more particularly are equal to 2. The anion X ′ is preferably a halide, preferably chloride, bromide or iodide, a (Ci-C 4 ) alkyl, an alkyl (CiC 4 ) sulfonate or an alkyl (Ci-C 4 ) aryl-sulfonate, methanesulfonate, a phosphate, a nitrate, a tosylate, an anion derived from organic acid such as an acetate or a lactate or any other anion compatible with ammonium with ester function. The anion X 'is more particularly a chloride, a methyl sulphate or an ethyl sulphate. The ammonium salts of formula (IX) in which: - R 22 denotes a methyl or ethyl group, - x and y are equal to 1, - z is 0 or 1, - r, s and t are equal to 2, - r2 and t2 are equal to 4, - rl and tl are equal to 0, - R23 is chosen from the group R26-C (= O) -; methyl, ethyl or C14-C22 hydrocarbon groups, the hydrogen atom, - R25 is chosen from the group R28-C (= O) -; the hydrogen atom, - R24, R26 and R28, identical or different, are chosen from C13-C17 hydrocarbon groups, linear or branched, saturated or unsaturated, and preferably from C13C17 alkyl and alkenyl groups, linear or branched, saturated or unsaturated. Advantageously, the hydrocarbon groups are linear. Mention may be made, among the compounds of formula (IX), of the salts, in particular the chloride or methyl sulfate of diacyloxyethyldimethylammonium, of diacyloxyethylhydroxyethyl methylammonium, of monoacyloxyethyldihydroxyethylmethyl ammonium, of triacyloxyethylmethylammonium, of monoacyloxyethyl hydroxyethyldimethylammonium, and. The acyl groups preferably have 14 to 18 carbon atoms and more particularly come from a vegetable oil such as palm or sunflower oil. When the compound contains several acyl groups, these can be the same or different. These products are obtained, for example, by direct esterification of triethanolamine, triisopropanolamine, alkyldiethanolamine or alkyldiisopropanolamine optionally oxyalkylenated on fatty acids, or on mixtures of fatty acids, in particular of plant or animal origin, or by transesterification of their methyl esters. This esterification can be followed by quaternization using an alkylating agent such as an alkyl halide, preferably methyl or ethyl, a dialkyl sulfate, preferably methyl or ethyl, methyl methanesulfonate, methyl paratoluenesulfonate, chlorohydrin, glycol or glycerol. Such compounds are for example sold under the names DEHYQUART® by the company HENKEL, STEPANQUAT® by the company STEPAN, NOXAMIUM® by the company CECA, REWOQUAT® WE 18 by the company Evonik. The first composition and the second composition which can be used according to the invention can contain, for example, a mixture of mono-, di- and triester salts of quaternary ammonium with a majority by weight of diester salts. It is also possible to use the ammonium salts containing at least one ester function described in patents US-A4874554 and US-A-4137180. One can also use behenoylhydroxypropyltrimethylammonium chloride, for example, offered by the company KAO under the name Quartamin BTC 131. Preferably, the ammonium salts containing at least one ester function contain two ester functions. The first cationic surfactant (s) of the first composition and the second cationic surfactant (s) of the second composition can also be chosen, independently of one another, from a mixture of the cationic surfactants of formula (VI) to (IX) above . Preferably, the first cationic surfactant (s) of the first composition and / or the second cationic surfactant (s) of the second composition are chosen from those of formula (VI) or (IX), and mixtures of these compounds, and more preferably among those of formula (VI), and mixtures of these compounds. In a particularly preferred manner, the first cationic surfactant (s) of the first composition and the second cationic surfactant (s) of the second composition are chosen, independently of each other, from the cetyltrimethylammonium, behenyltrimethylammonium salts, dipalmitoylethylhydroxyethyl methylammonium and their mixtures ; and in particular among the cetyltrimethylammonium and behenyltrimethylammonium salts and their mixtures. Very particularly preferably, the first cationic surfactant (s) of the first composition and the second cationic surfactant (s) of the second composition are methosulfate methosulfate chosen, independently of one another, from behenyltrimethylammonium chloride or methosulfate, chloride or cetyltrimethylammonium chloride, dipalmitoylethylhydroxyethylmethylammonium chloride or it, and mixtures thereof, and in particular from behenyltrimethylammonium chloride or methosulfate, cetyltrimethylammonium chloride or methosulfate, and mixtures thereof. Advantageously, the first cationic surfactant (s) of the first composition represent a total content of 0.05 to 15% by weight, preferably from 0.1 to 10% by weight, and more preferably from 1 to 5% by weight, per relative to the total weight of the first composition. Advantageously, the second cationic surfactant (s) of the second composition represent a total content of 0.05 to 10% by weight, preferably from 0.1 to 5% by weight, and more preferably from 0.5 to 2% by weight , relative to the total weight of the second composition. As indicated above, the second composition which can be used in the process according to the invention comprises water. Advantageously, the second composition comprises at least 15% by weight, preferably comprises at least 50% by weight, more preferably from 50 to 99.5% by weight, in particular from 70 to 99.5%, and even better still from 80 99.5% by weight of water, relative to the total weight of the second composition. The first and second compositions which can be used in the process according to the invention can also comprise, one and / or the other, one or more non-silicone fatty substances. By “fatty substance” is meant an organic compound insoluble in water at room temperature (25 ° C) and at atmospheric pressure (1 atm), that is to say with a solubility of less than 5% by weight, of preferably less than 1% by weight. They are generally soluble, under the same conditions of temperature and pressure, in organic solvents such as chloroform, ethanol, benzene, petroleum jelly oil or decamethylcyclopentasiloxane. By "non-silicone fatty substance" is meant a fatty substance whose structure does not comprise a silicon atom, therefore not comprising in particular a siloxane group. They generally have in their structure a hydrocarbon chain containing at least 6 carbon atoms. Advantageously, they are not oxyalkylenated and do not contain a -COOH function. The non-silicone fatty substance (s) which can be used according to the invention can be liquid or non-liquid at room temperature and at atmospheric pressure. The liquid fatty substances which can be used in the invention preferably have a viscosity less than or equal to 2 Pa.s, better less than or equal to 1 Pa.s and even better still less than or equal to 0.1 Pa.s at the temperature of 25 ° C and at a shear rate of 1 s' 1 . The liquid fatty substances which can be used according to the invention can in particular be chosen from liquid hydrocarbons, liquid fatty alcohols, liquid fatty esters, liquid fatty acids and mixtures of these compounds. By liquid hydrocarbon is meant a hydrocarbon composed only of carbon and hydrogen atoms, liquid at ordinary temperature (25 ° C) and at atmospheric pressure (760 mm Hg, or 1.013.10 5 Pa). More particularly, the liquid hydrocarbons are chosen from: - linear or branched C6-C6 alkanes, possibly cyclic. Examples include hexane, undecane, dodecane, tridecane and isoparaffins such as isohexadecane, isododecane and isodecane. - linear or branched hydrocarbons, of animal or synthetic mineral origin, of more than 16 carbon atoms, such as paraffin oils, and their derivatives, petroleum jelly, petroleum jelly oil, polydecenes, hydrogenated polyisobutene such than that sold under the Parléam® brand by NOF Corporation, squalane. Preferably, the liquid hydrocarbon (s) are chosen from paraffin oils, isoparaffins, petrolatum oil, undecane, tridecane, isododecane and their mixtures. In a very particularly preferred variant, the liquid hydrocarbon (s) are chosen from petroleum jelly oil, isoparaffins, isododecane and a mixture of undecane and tridecane. By liquid fatty alcohol is meant a non-glycerolated and non-oxyalkylenated fatty alcohol, liquid at ordinary temperature (25 ° C) and at atmospheric pressure (760 mm Hg, or 1.013.10 5 Pa). Preferably, the liquid fatty alcohols of the invention contain from 8 to 30 carbon atoms, in particular from 10 to 24 carbon atoms, and they can be saturated or unsaturated. The saturated liquid fatty alcohols are preferably branched. They may optionally include in their structure at least one aromatic or non-aromatic, preferably acyclic, cycle. More particularly, the liquid saturated fatty alcohols of the invention are chosen from octyldodecanol, decyl-2tetradecanol, isostearyl alcohol, 2-hexyldecanol. Octyldodecanol and decyl-2-tetradecanol are particularly preferred. Unsaturated liquid fatty alcohols have in their structure at least one double or triple bond, and preferably one or more double bonds. When several double bonds are present, they are preferably 2 or 3 in number and they may or may not be conjugated. These unsaturated fatty alcohols can be linear or branched. They may optionally include in their structure at least one aromatic cycle or not. They are preferably acyclic. More particularly, the liquid unsaturated fatty alcohols which can be used in the invention are chosen from oleic (or oleyl) alcohol, linoleic (or linoleyl) alcohol, linolenic (or linolenyl) alcohol and undecylenic alcohol. Oleic alcohol is particularly preferred. By liquid fatty ester is meant an ester derived from a fatty acid and / or a fatty alcohol, liquid at ordinary temperature (25 ° C) and at atmospheric pressure (760 mm Hg, or 1.013.10 5 Pa). More particularly, the liquid esters are chosen from the esters of saturated or unsaturated, linear or branched, linear or branched aliphatic mono- or polyacids, of C1-C26, and optionally hydroxylated saturated or unsaturated, linear or branched aliphatic mono- or polyalcohols, of C1 -C26, the total number of carbon atoms of the esters being greater than or equal to 10. Preferably, for monoalcohol esters, at least one of the alcohol or of the acid from which the esters of the invention are derived is branched. Among the monoesters of monoacids and monoalcohols, mention may be made of alkyl palmitates, in particular Ci-Cis, in particular ethyl and isopropyl, alkyl myristates especially in Ci-Cis, such as isopropyl myristate or ethyl, alkyl stearates, in particular Ci-Cis alkyl, in particular isocetyl stearate, ethyl-2-hexyl isononanoate, isodecyl neopentanoate, and isostearyl neopentanoate. One can also use the esters of di- or tricarboxylic acids in C3-C22, optionally hydroxylated, and of C1-C22 alcohols and the esters of mono-, di- or tricarboxylic acids optionally hydroxylated and of non-alcohols di-, tri-, tetra- or pentahydroxylated C4-C26 sugars Mention may in particular be made of diethyl sebacate, diisopropyl sebacate, diisopropyl adipate, di n-propyl adipate, dioctyl adipate, diisostearyl adipate, dioctyl maleate, undecylenate glyceryl, octyldodecyl stearoyl stearate, monoricinoleate of pentaerythrityl, the teteasononanoate of pentaerythrityl, the tetrapelargonate of pentaerythrityl, the tetraisostearate of pentaerythrityl, the tetraoctanoate of pentaerythrityl, propylene glycol dicaprylate, propylene glycol dicaprate, tridecyl erucate, triisopropyl citrate, triisoteearyl citrate, glyceryl trilactate, glyceryl trioctanoate, trioctyldodecyl citrate, citrate propylene glycol dioctanoate, neopentyl glycol diheptanoate, diethylene glycol diisanonate, polyethylene glycol distearates, and alkylmalates, in particular the (C6-Cjalkylmalates, in particular bis (Ci2-Ci3) alkylmalate. above, use is preferably made of ethyl, isopropyl, myristyl, cetyl, stearyl palmitates, ethyl-2-hexyl palmitate, 2-octyldecyl palmitate, alkyl myristates such as isopropyl, butyl, cetyl, 2-octyldodecyl myristate, hexyl stearate, propylene glycol dicaprylate, butyl stearate, isobutyl stearate; dioctyl, hexyl laurate, 2-hexyldecyl laurate, isononyl isononanate, cetyl octanoate, and bis (C12-C13) alkylmalate. Among the liquid fatty esters, it is possible to use esters and di-esters of sugars and of fatty acids in C6-C30, preferably in C12-C22 By “sugar” is meant oxygenated hydrocarbon compounds which have several alcohol functions, with or without aldehyde or ketone function, and which contain at least 4 carbon atoms. These sugars can be monosaccharides, oligosaccharides or polysaccharides. Preferably, these said sugars are chosen from sucrose, glucose, galactose, ribose, fucose, maltose, fructose, mannose, arabinose, xylose, lactose, and their derivatives, in particular alkylated, such than methylated derivatives like methylglucose. The sugar and fatty acid esters can be chosen in particular from the group comprising the esters or mixtures of sugar esters described above and of C6-C30, preferably C12-C22 fatty acids, linear or branched, saturated or unsaturated. If unsaturated, these compounds can have one to three carbon-carbon double bonds, conjugated or not. The esters according to this variant can also be chosen from mono-, di-, tri- and tetraesters, polyesters and their mixtures. These esters can be, for example, oleates, laurates, palmitates, myristates, behenates, cocoates, stearates, linoleates, linolenates, caprates, arachidonates, and their mixtures such as in particular the mixed oleo-palmitate, oleo-stearate, palmitostearate esters. More particularly, mono- and diesters are used, and in particular mono- or dioleates, stearates, behenates, oleopalmitates, linoleates, linolenates, oleostearates, sucrose, glucose or methylglucose or also methylglucose dioleate (Glucate® DO). Among the sugar esters, it is possible to use the pentaerythrityl esters, preferably pentaerythrityl tetra-iso-stearate, pentaerythrityl tetra-octanoate, the hexaesters of caprylic and capric acids in mixture with dipentaerythritol. Among the natural or synthetic esters of mono-, di- or triacids with glycerol, vegetable or synthetic oils can be used. More particularly, the said vegetable or synthetic oil (s) are chosen from triglyceride oils of vegetable or synthetic origin, such as liquid triglycerides of fatty acids containing from 6 to 30 carbon atoms such as heptanoic or octanoic acid triglycerides or alternatively , for example sesame, soybean, coffee, safflower, borage, sunflower, olive, almond, apricot, camellia, bambara pea, avocado, mango, bran oils rice, cotton, rose, kiwi seeds, sea buckthorn pulp, blueberry seeds, poppy seeds, orange seeds, sweet almonds, palm, copra, vernoia, marjoram , baobab, rapeseed, ximenia, pracaxi, the triglycerides of caprylic / capric acids such as those sold by the company STEARINERIES DUBOIS or those sold under the names Miglyol® 810, 812 and 818 by the company DYNAMIT NOBEL, oil jojoba, b oil shea butter. Preferably, as liquid esters which can be used according to the invention, plant-based triglycerides are used, in particular the oils chosen from avocado oil, olive oil, camellia oil, l apricot almond oil, and mixtures thereof and esters of C4-C22 di- or tricarboxylic acids and C1-C22 alcohols, in particular 1,3-propanediol dicaprylate. The term “fatty acid” means an unsalified fatty acid, that is to say that the fatty acid must not be in the form of generally soluble soap, that is to say that it must not be salified by a base. More particularly, the liquid fatty acids which can be used according to the invention are chosen from the acids of formula RCOOH, where R is a saturated or unsaturated radical, linear or branched, preferably comprising from 7 to 39 carbon atoms. Preferably, R is a C7-C29 alkyl or C7-C29 alkenyl group, better still a C12-C24 alkyl or C12-C24 alkenyl group. R can be substituted by one or more hydroxy groups and / or one or more carboxyl groups. Preferably, the liquid fatty acid (s) are chosen from oleic acid, linoleic acid and isostearic acid. The fatty substance (s) which can be used according to the invention can also be chosen from fatty substances which are not liquid at ambient temperature (25 ° C.) and at atmospheric pressure (760 mm Hg, ie 1.013 × 10 5 Pa). The term “non-liquid fatty substance” is preferably understood to mean a solid compound or a compound having a viscosity greater than 2 Pa.s at a temperature of 25 ° C. and at a shear rate of 1 s ′ 1 . More particularly, the non-silicone “non-liquid” fatty substances are chosen from fatty alcohols, fatty acid and / or fatty alcohol esters, non-silicone waxes, fatty amines and ethers, which are non-liquid and preferably solid. More particularly, the non-liquid fatty alcohols which can be used according to the invention are chosen from saturated or unsaturated, linear or branched alcohols, containing from 8 to 30 carbon atoms. Preferably, there may be mentioned for example myristic alcohol, cetyl alcohol, stearyl alcohol, and their mixture (cetylstearyl alcohol in particular). More particularly, myristic alcohol is used. The fatty acid ester (s) and / or non-liquid fatty alcohols which can be used according to the invention are generally chosen from solid esters derived from C9-C26 fatty acids and from C9-C26 fatty alcohols Preferably, examples that may be mentioned include octyldodecyl behenate, isoketyl behenate, cetyl lactate, stearyl octanoate, octyl octanoate, cetyl octanoate, oleate decyl, myristyl stearate, octyl palmitate, octyl pelargonate, octyl stearate, alkyl myristates such as cetyl, myristyl or stearyl myristate, and hexyl stearate . The non-silicone wax (es) are chosen in particular from Carnauba wax, Candelila wax, Alfa wax, paraffin wax, ozokerite, vegetable waxes such as olive wax, rice wax , hydrogenated jojoba wax or absolute flower waxes such as essential blackcurrant flower wax sold by the company BERTIN (France), animal waxes such as beeswax, or modified beeswax (cerabellina) and ceramides or the like. Ceramides or ceramide analogs, such as natural or synthetic glycoceramides can be chosen from the compounds corresponding to the following formula (X): R'CHOH — CH — CH 2 OR NH C = O R '(X) in which: - R 'denotes an alkyl radical, linear or branched, saturated or unsaturated, derived from C14-C30 fatty acids, this radical possibly being substituted by a hydroxyl group in the alpha position, or a hydroxyl group in the omega position esterified by an acid saturated or unsaturated C16-C30 fat; - R ”denotes a hydrogen atom or a (glycosyl) n, (galactosyl) m or sulfogalactosyl radical, in which n is an integer varying from 1 to 4 and m is an integer varying from 1 to 8; - R ’” denotes a C 15 -C 26 hydrocarbon radical, saturated or unsaturated in the alpha position, this radical possibly being substituted by one or more C 1 -C 14 alkyl radicals; it being understood that in the case of natural ceramides or glycoceramides, R ′ ”can also denote an alpha-hydroxyalkyl radical in Ci 5 -C 26, the hydroxyl group being optionally esterified by an alpha-hydroxy acid in C16-C30 · The preferred ceramides in the context of the present invention are those described by DOWNING in Arch. Dermatol, Vol. 123, 13811384, 1987, or those described in French patent FR 2,673,179. The ceramide (s) more particularly preferred according to the invention are the compounds for which R ′ denotes a saturated or unsaturated alkyl derived from C16-C22 fatty acids, R ″ denotes a hydrogen atom and R ″ ″ denotes a linear radical saturated with C15. Preferably, the following compounds can be chosen in particular: N-linoleoyldihydrosphingosine, Noleoyldihydrosphingosine, N-palmitoyldihydrosphingosine, Nstearoyldihydrosphingosine, N-behenoyldihydrosphingosine and a mixture of these compounds. Even more preferably, ceramides are used for which R 'denotes a saturated or unsaturated alkyl radical derived from fatty acids, R ”denotes a galactosyl or sulfogalactosyl radical and R'” denotes a group -CH = CH- (CH 2 ) i2 -CH3. Other waxes or waxy raw materials which can be used according to the invention are in particular marine waxes such as those sold by the company SOPHIM under the reference M82, polyethylene or polyolefin waxes in general. The non-liquid fatty ethers which can be used according to the invention are chosen from dialkyl ethers, in particular diketyl ether and distearyl ether, alone or as a mixture. Preferably, the non-silicone fatty substance (s) which can be used according to the invention are chosen from hydrocarbons, in particular linear or branched C6-Ci6 alkanes and linear or branched hydrocarbons, of animal or synthetic mineral origin, more than 16 carbon atoms, such as paraffin oils, and their derivatives, petrolatum, petrolatum oil; fatty acid esters, in particular oils of vegetable origin and esters of C4-C22 di- or tricarboxylic acids and C1-C22 alcohols, these esters being more preferably chosen from triglycerides of vegetable origin , liquid fatty alcohols, solid fatty alcohols and their mixtures. When they are present in the first composition which can be used according to the process of the invention, the non-silicone fatty substance (s) generally represent from 1 to 50% by weight, preferably from 2 to 30% by weight, more preferably from 10 to 30 % by weight relative to the total weight of the first composition. When they are present in the second composition which can be used according to the process of the invention, the non-silicone fatty substance (s) generally represent from 0.001 to 10% by weight, preferably from 0.01 to 1% by weight, more preferably from 0 0.05 to 0.5% by weight relative to the total weight of the second composition. In a particularly preferred embodiment of the invention, the first composition comprises one or more non-silicone fatty substances, preferably selected from fatty alcohols, C 8 -C 2 8, preferably C10-C24, fatty esters , preferably chosen from (C6-Ci 8 ) alkylmalates, and in particular bis (Ci2Cnjalkylmalate). Preferably in this embodiment, the first composition comprises at least one (C6-Ci 8 ) alkylmalate, in particular bis (Ci2-Ci3) alkylmalate. Advantageously, the second composition which can be used in the process according to the invention can comprise one or more non-amino-non-oxyalkylenated silicones. The first and second compositions which can be used in the process according to the invention may also comprise, one and / or the other, one or more surfactants chosen from nonionic, anionic, and amphoteric or zwitterionic surfactants. The first and second compositions which can be used in the process according to the invention can also comprise, one and / or the other, one or more organic solvents. Preferably, the organic solvent (s) are chosen from non-aromatic Ci-C6 alcohols such as ethyl alcohol, isopropyl alcohol, or aromatic alcohols such as benzyl alcohol and phenylethyl alcohol; polyols such as propylene glycol, butylene glycol, glycerol, or polyol ethers such as, for example, the monomethyl, monoethyl and monobutyl ethers of ethylene glycol, propylene glycol or its ethers such as, for example, the monomethyl ether of propylene glycol, butylene glycol, dipropylene glycol as well as the alkyl ethers of diethylene glycol such as, for example, monoethyl ether or monobutyl ether of diethylene glycol. In a particularly preferred manner, the first composition which can be used in the process according to the invention comprises one or more organic solvents, preferably chosen from ethyl alcohol, propylene glycol and their mixtures. When they are present in the first composition which can be used according to the process of the invention, the organic solvent (s) generally represent a total content of 20 to 95% by weight, preferably from 45 to 85% by weight, more preferably from 55 at 80% by weight relative to the total weight of the first composition. When they are present in the second composition which can be used according to the process of the invention, the organic solvent (s) generally represent a total content of 0.1 to 15% by weight, preferably from 1 to 10% by weight, relative to the total weight of the second composition. In a particular embodiment, the first and / or the second compositions which can be used according to the process of the invention can comprise one or more cationic polymers. Preferably in this particular embodiment, the second composition comprises one or more cationic polymers. The term “cationic polymer” means any polymer comprising cationic groups and / or groups that can be ionized into cationic groups. Preferably, the cationic polymer is hydrophilic or amphiphilic. The preferred cationic polymers are chosen from those which contain units comprising primary, secondary, tertiary and / or quaternary amine groups which can either be part of the main polymer chain, or be carried by a lateral substituent directly connected thereto. More particularly, the cationic polymers which can be used according to the present invention are chosen from polymers of the polyamine, polyaminoamide and quaternary polyammonium type, polyalkyleneimines and their mixtures. The polymers of the polyamine, polyaminoamide, quaternary polyammonium type, which can be used in accordance with the present invention, which may be mentioned in particular, are those described in French patents 2,505,348 or 2,542,997. Among the cationic polymer (s) which can be used according to the invention, there may be mentioned: (1) vinylpyrrolidone / (meth) acrylate dialkylamino-alkyl copolymers, quaternized or not, (2) polymers consisting of piperazinyl units and divalent alkylene or hydroxyalkylene groups with straight or branched chains, optionally interrupted by oxygen atoms, sulfur, nitrogen or by aromatic or heterocyclic rings, as well as the oxidation and / or quaternization products of these polymers. Such polymers are described in particular in French patents 2,162,025 and 2,280,361; (3) water-soluble polyaminoamides prepared in particular by polycondensation of an acidic compound with a polyamine; these polyaminoamides can be crosslinked with an epihalohydrin, a diepoxide, a dianhydride, an unsaturated dianhydride, a bis-unsaturated derivative, a bis-halohydrin, a bis-azetidinium, a bis-haloacyldiamine, a bis-halide of alkyl or also with an oligomer resulting from the reaction of a bifunctional compound reactive with a bis-halohydrin, a bis-azetidinium, a bishaloacyldiamine, an alkyl bis-halide, a epilhalohydrin, a diepoxide or a bisunsaturated derivative; the crosslinking agent being used in proportions ranging from 0.025 to 0.35 mol per amine group of the polyaminoamide; these polyaminoamides can be alkylated or if they contain one or more tertiary amine functions, quaternized. Such polymers are described in particular in French patents 2 252 840 and 2 368 508; (4) polyaminoamide derivatives resulting from the condensation of polyalkylene polyamines with polycarboxylic acids followed by alkylation by bifunctional agents. Mention may be made, for example, of the adipic acid / diakylaminohydroxyalkyl-dialkylene-triamine polymers in which the alkyl group contains from 1 to 4 carbon atoms and preferably denotes methyl, ethyl, propyl. Such polymers are described in particular in French patent 1,583,363. (5) polymers obtained by reaction of a polyalkylene polyamine comprising two primary amine groups and at least one secondary amine group with a dicarboxylic acid chosen from diglycolic acid and saturated aliphatic dicarboxylic acids having from 3 to 8 carbon atoms. The molar ratio between the polyalkylene polylamine and the dicarboxylic acid being between 0.8: 1 and 1.4: 1; the resulting polyaminoamide being reacted with epichlorohydrin in a molar ratio of epichlorohydrin relative to the secondary amine group of the polyaminoamide of between 0.5: 1 and 1.8: 1. Such polymers are described in particular in the patents 3,227,615 and 2,961,347. (6) alkyldiallylamine or dialkyldiallylammonium cyclopolymers such as homopolymers or copolymers comprising units corresponding to formulas (XI) or (XII): H CH H NOT (xi) (xii) in which, - k and t are equal to 0 or 1, the sum k + t being equal to 1; - R9 denotes a hydrogen atom or a methyl group; R7 and Rg, independently of one another, denote an alkyl group having from 1 to 22 carbon atoms, a hydroxyalkyl group in which the alkyl group preferably has 1 to 5 carbon atoms, a lower amidoalkyl group, or R7 and Rg may denote, jointly with the nitrogen atom to which they are attached, heterocyclic groups, such as piperidinyl or morpholinyl; and - Y 'is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate, phosphate. These polymers are described in particular in French patent 2,080,759 and in its certificate of addition 2,190,406. Mention may be made, for example, of the homopolymer of diallyldimethylammonium chloride sold under the name "MERQUAT® 100" by the company NALCO (LUBRIZOL) and the copolymers of diallyldimethylammonium chloride and of acrylamide. (7) quaternary diammonium polycondensates containing recurring units corresponding to formula (XIII): -NA 1 -NB r (xiii) in which, - Rio, Ru, R12 and R13, identical or different, represent aliphatic, alicyclic, or aryl aliphatic groups containing from 1 to 20 carbon atoms or lower aliphatic hydroxyalkyl groups, or alternatively R 10 , Ru, R12 and R13, together or separately, constitute with the nitrogen atoms to which they are attached heterocycles optionally containing a second heteroatom other than nitrogen, or else R 10 , R11, R12 and R13 represent a linear or branched C1 to C6 alkyl group, substituted by a nitrile, ester, acyl, amide or -CO-ORD or -CO-NH-RD group where R is an alkylene group and D a quaternary ammonium group; - Ai and Bi represent polymethylenic groups containing from 2 to 20 carbon atoms, which may be linear or branched, saturated or unsaturated, and which may contain, linked to or intercalated in the main chain, one or more aromatic rings, or one or more oxygen, sulfur or sulfoxide, sulfone, disulfide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide or ester groups, and - X 'denotes an anion derived from a mineral or organic acid; Ai, Rio and R12 can form with the two nitrogen atoms to which they are attached a piperazine ring; in addition, if Ai denotes a linear or branched, saturated or unsaturated alkylene or hydroxyalkylene group, Bi can also denote a group - (CH 2 ) n -CO-DOC- (CH 2 ) n - in which D denotes: a) a glycol residue of formula: -O-Z-O-, where Z denotes a linear or branched hydrocarbon group or a group corresponding to one of the following formulas: - (CH2-CH 2 -O) x -CH2-CH 2 3064476 - [CH 2 -CH (CH 3 ) -O] y -CH 2 -CH (CH 3 ) where x and y denote an integer from 1 to 4, representing a defined and unique degree of polymerization or any number of 1 to 4 representing an average degree of polymerization; b) a bis-secondary diamine residue such as a piperazine derivative; c) a bis-primary diamine residue of formula: -NH-Y-NH-, where Y denotes a linear or branched hydrocarbon group, or else the bivalent group -CH 2 -CH 2 -SS-CH 2 -CH 2 -; d) a ureylene group of formula: -NH-CO-NH-. Preferably, X 'is an anion such as chloride or bromide. These polymers have a number average molecular weight generally between 1000 and 100,000 g / mol. Polymers of this type are described in particular in French patents numbers 2 320 330, 2 270 846, 2 316 271, 2 336 434 and 2 413 907 and US patents numbers 2 273 780, 2 375 853, 2 388 614, 2 454,547, 3,206,462, 2,261,002, 2,271,378, 3,874,870, 4,001,432, 3,929,990, 3,966,904, 4,005 193, 4,025,617, 4,025,627, 4,025,653, 4,026,945 and 4,027,020. It is possible to use more particularly the polymers which consist of recurring units corresponding to formula (XIV): -N- (CH 2 ) —N- (CH 2 ) - in which, - R14, Ris, Riô and R17, identical or different, denote an alkyl or hydroxyalkyl group having from 1 to 4 carbon atoms approximately, - n and p are whole numbers varying from approximately 2 to 20, and - X 'is an anion derived from a mineral or organic acid. A particularly preferred compound of formula (XIV) is that for which Ri 4 , Ris, Ri6 and R17 represent a methyl group and n = 3, p = 6 and X = Cl, called “Hexadimethrine chloride” according to the INCI nomenclature (CTFA) . (8) quaternary polyammonium polycondensates consisting of units of formula (XV): ^ 18 ^ 20 - N— (CH 2 ) r —NH CO- (CH 2 ) —CO-NH— (CH 2 ) s —N — ΑΧ r RX ^ 19 ^ 21 A (xv) in which, - Ri8, R19, R20 and R21, identical or different, represent a hydrogen atom or a methyl, ethyl, propyl, βhydroxyethyl, β-hydroxypropyl group or -CFUCH ^ OCFUCfDpOH, where p is 0 or an integer between 1 and 6, provided that Ris, R19, R20 and R21 do not simultaneously represent a hydrogen atom, - r and s, identical or different, are whole numbers between 1 and 6, - q is equal to 0 or to an integer between 1 and 34, - X denotes a halogen atom, and - A denotes a group of a dihalide or preferably represents -CH2-CH2-O-CH2-CH2-. Such compounds are described in particular in patent application EP-A-122 324. Mention may, for example, be made, among these, of the products “Mirapol® A 15”, “Mirapol® ADI”, “Mirapol® AZ1” and “Mirapol® 175” sold by the company Miranol. (9) homopolymers or copolymers derived from acrylic or methacrylic acids and comprising units (XVI), (XVII) and / or (XVIII): R. '22 o = c AT. R. '26 R. '27 (xvi) R. ‘23 (XVII) and / or o = c NH R. '23 (XVIII) in which, - R22 independently denotes H or CH 3 , - A 2 independently denotes a linear or branched alkyl group of 1 to 6 carbon atoms, or a hydroxyalkyl group of 1 to 4 carbon atoms, R23, R24, R25, identical or different, independently denote an alkyl group of 1 to 18 carbon atoms, or a benzyl group, - R26 and R27 represent a hydrogen atom or an alkyl group of 1 to 6 carbon atoms, and - X2 ’denotes an anion, for example methosulfate or halide such as chloride or bromide. The comonomer (s) which can be used in the preparation of the corresponding copolymers belong to the family of acrylamides, methacrylamides, diacetone-acrylamides, acrylamides and methacrylamides substituted with nitrogen by lower alkyls, alkyl esters, acrylic or methacrylic acids, vinylpyrrolidone or vinyl esters. (10) Quaternary polymers of vinylpyrrolidone and vinylimidazole. (11) Crosslinked polymers of methacryloyloxyalkyl (Ci-C4) trialkyl (Ci-C4) ammonium salts such as the polymers obtained by homopolymerization of dimethylaminoethyl methacrylate quaternized by methyl chloride, or by copolymerization of acrylamide with methacrylate of dimethylaminoethyl quaternized with methyl chloride, the homopolymerization or copolymerization being followed by crosslinking with an olefinically unsaturated compound, in particular methylene-bis-acrylamide, (12) mixtures thereof. Other cationic polymers which can be used in the context of the invention are polyalkyleneimines, in particular polyethyleneimines, polymers containing vinylpyridine or vinylpyridinium units, condensates of polyamines and epichlorohydrin, quaternary polyuretylenes and chitin derivatives. Among all the cationic polymers capable of being used in the context of the present invention, it is preferred to use those chosen from families (6), (7), (8), (9) and (11), such as defined above, and more preferably those chosen from the family (7) as defined above. When the first and / or the second composition which can be used in the process of the invention comprise one or more cationic polymers, the total content of cationic polymer (s) is between 0.01 and 5% by weight, preferably between 0.05 and 3% by weight, and more preferably between 0.1 and 2% by weight, relative to the total weight of the composition containing them. The pH of the first composition which can be used in the process of the invention is generally between 2 and 7, preferably between 2.5 and 6, even better between 3 and 5.5 and preferably between 3.5 and 5. The pH of the second composition which can be used in the process of the invention is generally between 1 and 7, preferably between 2 and 6, even better between 2.5 and 5, and preferably between 3 and 4.5. The pH of the first and second compositions which can be used in the process of the invention can be adjusted and / or stabilized by means of basifying agents and / or acidifying agents, well known to those skilled in the art. As alkalizing agent, there may be mentioned in particular ammonia, alkali carbonates or bicarbonates, organic amines whose pKb at 25 ° C is less than 12, and in particular less than 10, even more advantageously less than 6; among the salts of the amines mentioned above with acids such as carbonic acid, hydrochloric acid, it should be noted that this is the pKb corresponding to the highest basicity function. Preferably, the amines are chosen from alkanolamines, comprising in particular a primary, secondary or tertiary amine function, and one or more alkyl groups, linear or branched, in Ci-Cg carrying one or more hydroxyl radicals; among oxyethylenated and / or oxypropylenated ethylenediamines, among amino acids and the compounds of the following formula: Rx Rz / NW-N R y Rt in which W is a C 1 -C 6 alkylene radical optionally substituted by a hydroxyl group or a C 1 -C 6 alkyl radical; Rx, Ry, Rz and Rt, identical or different, represent a hydrogen atom, a C1-C6 alkyl or C1-C6 hydroxyalkyl radical, a C1-C6 aminoalkyl radical. Mention may in particular be made, as acidifying agent, of hydrochloric acid, (ortho) phosphoric acid, sulfuric acid, boric acid, and also carboxylic acids such as, for example, acetic acid, lactic, citric acid, or sulfonic acids. The first and second compositions which can be used in the process according to the invention may also contain additives such as polymers, natural or synthetic, anionic, amphoteric or zwitterionic, non-ionic, associative or not, non-polymeric thickeners such as electrolytes, sugars, nacrants, opacifiers, sunscreens, vitamins or provitamins, perfumes, organic or mineral particles, preservatives. A person skilled in the art will take care to choose any additives and their quantity so that they do not harm the properties of the compositions which can be used in the process of the present invention. These additives can be present in the compositions which can be used in the process according to the invention in an amount ranging from 0 to 50% by weight relative to the total weight of the composition containing them. In a particular embodiment of the invention, the second composition comprises one or more vitamins. In another particular embodiment of the invention, the second composition comprises one or more cationic polymers. In this other particular embodiment of the invention, the cationic polymer (s) are preferably chosen from those mentioned above. The first and second compositions which can be used in the process according to the invention are generally transparent. The first and second compositions which can be used in the process according to the invention are generally liquid. As described above, the method according to the invention comprises a step of mixing the first and second compositions as described above, so as to obtain a final cosmetic composition. Preferably, the method according to the invention comprises a step of mixing only the first and second compositions as described above, so as to obtain a final cosmetic composition. In the process according to the invention, the first and second compositions are generally mixed in a first composition / second composition weight ratio ranging from 0.2 to 5, preferably ranging from 0.3 to 3, more preferably ranging from 0, 5 to 1.5, and in particular the weight ratio is equal to 1/1. In a particular embodiment of the method according to the invention, the mixing step is carried out just before the application step, preferably less than two hours before, more preferably less than an hour before, and again better less than 15 minutes before the application stage. The final cosmetic composition obtained is generally opaque and has a thickened texture. This texture makes it possible in particular to facilitate the application of the final composition to the keratin fibers. Thus, the method according to the invention then comprises a step of applying the final cosmetic composition to the keratin fibers. Preferably, once the final cosmetic composition has been spread, it is left on the keratin fibers for a period ranging from 2 to 15 minutes. The final cosmetic composition can in particular be applied before and / or after a shampoo, a coloring, in particular a coloring by oxidation, a perm, a straightening, or any other treatment of the hair. The composition can then be rinsed or not after application, preferably rinsed. The present invention also relates to a kit comprising at least two compartments: a first compartment comprising a first composition as defined above, - a second compartment comprising a second composition as defined above. Thus, each of the compositions is packaged separately, in particular in a bottle or a pump bottle, and the two compartments can be separated or grouped, preferably grouped. At the time of the cosmetic treatment, the user will mix at least said first composition with said second composition, for example in a suitable container, preferably in the weight ratio as indicated above. The final cosmetic composition obtained is ready to be then applied to the keratin fibers. Finally, the subject of the invention is a cosmetic composition for the cosmetic treatment of keratin fibers comprising: i) one or more non-amino oxyalkylenated silicones, preferably non-amino oxyethylenated silicones, ii) one or more first cationic surfactants, iii) one or more second cationic surfactants different from the cationic surfactants (ii), iv) of water. Preferably, the composition according to the invention is the final cosmetic composition resulting from the mixture of the first and the second compositions which can be used in the process according to the invention as described above. Thus, preferably, the cosmetic composition according to the invention has one or more of the characteristics of the first and second compositions as described above, in particular as regards the non-amino oxyalkylenated silicone (s) of the first composition, the or the first cationic surfactants of the first composition, and the second cationic surfactant (s) of the second composition. Preferably, the non-amino oxyalkylenated silicone (s) of the cosmetic composition according to the invention represent from 0.001 to 8.5% by weight, preferably from 0.008 to 4.5% by weight, and more preferably from 0.01 to 2% by weight, relative to the total weight of the cosmetic composition. Preferably, the first cationic surfactant (s) (ii) of the cosmetic composition according to the invention represent 0.0005 to 12.5% by weight, preferably from 0.001 to 8.5% by weight, and more preferably from 0.003 to 4.5% by weight, better still from 0.1 to 4% by weight, relative to the total weight of the cosmetic composition. Preferably, the second cationic surfactant or surfactants (iii) different from the cationic surfactants (ii) of the cosmetic composition according to the invention represent from 0.0005 to 12.5% by weight, preferably from 0.001 to 8.5% by weight, and more preferably from 0.003 to 4.5% by weight, better still from 0.1 to 4% by weight relative to the total weight of the cosmetic composition. This composition finds, in particular, a particularly advantageous application in the hair field, in particular for the care and / or conditioning of the hair. Advantageously, it is in the form of a conditioning product or also in the form of a hair gel, a lotion, a cream or in the form of a mask, in particular for the care and / or the conditioning of keratin fibers. This composition generally has a thickened texture. This composition is generally opaque. The following examples illustrate the present invention and should not be considered in any way as limiting the invention. EXAMPLES Example 1: Preparation of a first composition which can be used in the process according to the invention ("base" composition) Composition A was prepared according to Table 1 below by mixing the ingredients at the levels indicated in grams of active material. Table 1 Basic composition AT Behenyltrimethylammonium methosulfate 1.6 Cetyltrimethylammonium chloride 1.8 PH agent Qs pH 4.5 ± 0.5 Myristic alcohol 7.0 Caprylic-capric acid triglycerides 7.3 Bis (Ci2-Ci3) alkyl-2-hydroxybutandioate 0.8 Methyl glucoside oxypropoxyl (10 OP) 0.9 Propylene glycol 15 Oxyethylenated polydimethylsiloxane 14 OE 1 Perfume qs Ethanol 50 Water qs 100 g Example 2: preparation of second compositions which can be used in the process according to the invention ("booster" compositions) The compositions B1 to Cl were prepared according to Table 2 below by mixing the ingredients at the levels indicated in grams of active material. Table 2 Booster compositions B1 Cl PH agent qs pH 3.5 ± 0.5 qs pH 3.5 ± 0.5 Preservatives qs qs Mixture of plant-based amino acids - 0.1 Hexadimethrin chloride - 1.35 Amodimethicone (BELSIL ADM LOG 1 from Wacker) - 2.25 Glycerin - 6.8 Chloridecetyltrimethylammonium 0.75 1.5 Pyridoxine hydrochloride 0.1 - D-Biotin 0.01 - Water qs 100 g qs 100 g Example 3 Preparation and Use of the Final Compositions 5 Usable in the Process According to the Invention The “base” composition A was mixed with each of the “booster” compositions B1 to Cl in a weight ratio of 1/1 to respectively form the final compositions B2 to C2. The final compositions are obtained by mixing using a spatula of the two compositions and, after mixing, form masks (compositions in the form of a cream). The compositions are applied to the hair at a rate of 15 12 g of final composition for the whole of the hair, then left on the hair for 5 minutes. The hair is then rinsed and dried. The final composition B2 leads to good performance in terms of detangling, smoothing to the touch and coating the hair. The final composition C2 leads to good performance in terms of detangling, smoothing to the touch and coating the hair. Example 4: instrumental evaluation of the compositions 4.1 Composition B2 Composition B2 was evaluated in terms of resistance to breakage on brushing, compared to a composition B’2 resulting from the mixture of composition A with water, in a 1/1 ratio. Each of the final compositions is applied to 10 locks of medium-sensitized hair (alkaline solubility 21.6%) measuring 26 cm and weighing 2.7 g previously washed and towel-dried, at the rate of 1.08 g of composition per lock of hair. After 5 minutes of laying, the locks are rinsed. We then brush the locks in a standardized way: the hair broken during the operation is carefully collected and weighed. The lower the amount of broken hair, the higher the resistance to brushing. Below are the means of the relative masses of broken hair (expressed in mg / g) during brushing for each of the compositions. Relative mass (mg / g) Invention B2 (from the mixture of A + Bl) 18.3 Comparative B’2 (from mixture A + water) 41.8 Composition B2 has a 56.2% improvement in resistance to breakage while brushing compared with comparative composition B’2. 4.2 Composition C2 Composition C2 was evaluated for its influence on the resistance of locks of hair, using a flexabrasion test. The flexabrasion test simulates the wear of a hair to measure its resistance. The device reproduces the real conditions of the stresses inflicted during combing or brushing: extension (when the comb stretches the hair), abrasion (when the fibers rub on each other or on the teeth of the comb) and bending (when the hair is wrapped around the comb). A hair stretched thanks to a weight fixed at one of its ends, slides by bending on a comb tooth. A device drives it back and forth, with a given amplitude and frequency. The resistance of the hair is characterized by the duration and / or the number of cycles at the end of which the hair, subjected to this stress, breaks. The duration before breakage and / or the number of cycles before breakage is all the more higher as the hair is resistant. Clean locks of hair weighing 2.7 g and measuring 26 cm are treated on the one hand with composition C2 from the mixture of compositions A and Cl, and on the other hand with a composition C'2 from the mixture of the composition A with water, in a ratio 1/1 in both cases, at a rate of 1.08 g of composition per lock of hair. After a 5-minute break, the locks are rinsed and dried. This treatment (application, rinsing, drying) is repeated a total of times. After the 5 th treatment is taken every strand of hair 25 to proceed to flexabrasion test on each hair. Below are presented the median values of the number of cycles and duration at the time of breakage (on 25 hairs). Number of cycles Duration (in seconds) Treatment with C2(invention) - 5 applications 388.5 777 Treatment with C’2(comparison) - 5 applications 290 580 It can be seen that the use of the composition C2 leads to a higher number of cycles and a duration before breakage than the use of the comparative composition C’2. Composition C2 therefore very clearly improves the resistance of the hair.
权利要求:
Claims (16) [1" id="c-fr-0001] 1. A method of cosmetic treatment of keratin fibers, preferably human keratin fibers such as the hair, comprising: (i) a mixing step of at least: a first composition comprising one or more oxyalkylenated silicones and one or more first cationic surfactants, and - A second composition comprising water and one or more second cationic surfactants, so as to obtain a final cosmetic composition, then (ii) a step of applying the final cosmetic composition to the keratin fibers. [2" id="c-fr-0002] 2. Method according to claim 1, characterized in that the first composition comprises less than 10% by weight, and preferably less than 9% by weight of water relative to the total weight of the composition. [3" id="c-fr-0003] 3. Method according to claim 1 or 2, characterized in that the oxyalkylenated silicone (s) of the first composition are chosen from the compounds of general formulas (I), (II), (III), (IV) or (V) following: Ç H 3 - ch 3- h Ç H 3 η - That 3 - ch 3R 2 - Si-0 Yes PJ Bi n Bi ΓΊ I - Si-R 2 U ch 3 L Ri 0 - r 2m L ch 3 J n CH 3 (I) (Π) (III) R 3-Si Çh 3 o— If - (OC 2 H 4 ) a (OC 3 H 6 ) b OR I - x ch 3 (IV) formulas (I), (II), (III) and (IV) in which: - Ri, identical or different, represents an alkyl radical, linear or branched, C1-C30 or phenyl, - R2, identical or different, represents a radical C c H 2 cO (C2H 4 O) a (C 3 H 6 O) b -R 5 or a radical -C c H 2 cO- (C 4 H 8 O) a -R 5 , - R3 and R 4 , identical or different, denote an alkyl radical, linear or branched, Ci to C12, and preferably the methyl radical, - R5, identical or different, is chosen from a hydrogen atom, an alkyl radical, linear or branched, from 1 to 12 carbon atoms, an alkoxy radical, linear or branched, from 1 to 6 carbon atoms, a radical acyl, linear or branched, from 2 to 30 carbon atoms, a hydroxyl radical, -SO3M, C1-C6 aminoalkoxy optionally substituted on the amine, C2-C6 aminoacyl optionally substituted on the amine, -NHCH2CH2COOM, -N (CH2CH 2 COOM) 2, aminoalkyl optionally substituted on the amine and on the alkyl chain, carboxyacyl in C2-C30, a group optionally substituted by one or two substituted aminoalkyl radicals, -CO (CH 2 ) d COOM, -COCHR 7 (CH 2 ) d COOM, -NHCO (CH 2 ) d OH, -NH 3 Y, a phosphate group, - M, identical or different, denotes a hydrogen atom, Na, K, Li, NH 4 or an organic amine, - R 7 denotes a hydrogen atom or an SO 3 M radical, - d varies from 1 to 10, - m varies from 0 to 20, - n varies from 0 to 500, - o varies from 0 to 20, - p varies from 1 to 50, - a varies from 0 to 50, - b varies from 0 to 50, - a + b is greater than or equal to 2, - c varies from 0 to 4, - x varies from 1 to 100, - Y represents a monovalent inorganic or organic anion such as halide, sulphate, carboxylate, provided that when the silicone is of formula (II) with R5 denoting hydrogen then n is greater than 12; ([Z (R 2 SiO) q R ' 2 SiZO] [(C „H 2n O) r ]) s (V) formula (V) in which: - R 2 and R ' 2 , identical or different, represent a monovalent hydrocarbon radical, - n is an integer ranging from 2 to 4, q is a number greater than or equal to 4, preferably between 4 and 200 and even more particularly between 4 and 100, r is a number greater than or equal to 4, preferably between 4 and 200 and even more particularly between 5 and 100, - s is a number greater than or equal to 4, preferably between 4 and 1000 and even more particularly between 5 and 300, Z represents a divalent organic group which is linked to the adjacent silicon atom by a carbon-silicon bond and to a polyoxyalkylene block by an oxygen atom, the average molecular weight of each siloxane block is between approximately 400 and approximately 10,000, that of each polyoxyalkylene block being between approximately 300 and approximately 10,000, the siloxane blocks represent from about 10% to about 95% by weight of the block copolymer, - The number average molecular weight of the block copolymer varies from 2,500 to 1,000,000 and preferably between 3,000 and 200,000 and even more particularly between 6,000 and 100,000. [4" id="c-fr-0004] 4. Method according to claim 3, characterized in that the oxyalkylenated silicone (s) of the first composition are chosen from non-amino oxyethylenated silicones, preferably of formula (II) in which: - R.2, identical or different, represents a radical -CcH 2c -O (C2H 4 O) a (C 3 H 6 O) b -R 5 , - c is equal to 2 or 3, - Ri denotes the methyl radical, - Rs represents a hydrogen atom, - a varies from 2 to 25 and more particularly from 2 to 20, - b is equal to 0, - n varies from 0 to 100, - p varies from 1 to 20. [5" id="c-fr-0005] 5. Method according to any one of the preceding claims, characterized in that the oxyalkylenated silicone (s) of the first composition represent from 0.01 to 10% by weight, preferably from 0.05 to 5% by weight, and more preferably from 0.1 to 2% by weight, relative to the total weight of the first composition. [6" id="c-fr-0006] 6. Method according to any one of the preceding claims, characterized in that the first cationic surfactant (s) of the first composition and the second cationic surfactant (s) of the second composition are chosen, independently of one another, from the following compounds : the quaternary ammonium salts of formula (VI) below: (VI) Formula (VI) in which: the groups R 8 to Ru, which may be identical or different, represent an aliphatic group, linear or branched, comprising from 1 to 30 carbon atoms, or an aromatic group such as aryl or alkylaryl, at least one of the groups R 8 to Ru denoting an aliphatic radical, linear or branched, comprising from 8 to 30 carbon atoms, preferably from 12 to 24 carbon atoms, X ′ is an anion chosen from the group of halides, phosphates, acetates, lactates, (Ci-C4) alkyl sulfates, (Ci-C4) alkyl - or (Ci-C4) alkyl aryl sulfonates, - the quaternary ammonium salts of imidazoline, such as for example those of formula (VII) below: R. (VII) Formula (VII) in which: R12 represents an alkenyl or alkyl group comprising from 8 to 30 carbon atoms, for example derived from tallow fatty acids, R13 represents a hydrogen atom, an alkyl group CiC 4 or an alkenyl or alkyl group having from 8 to 30 carbon atoms, Ri4 represents a C1-C4 alkyl group, 2+ 2X Ris represents a hydrogen atom, an alkyl group CiC 4, X ′ is an anion chosen from the group of halides, phosphates, acetates, lactates, alkyl sulfates, alkyl- or alkylarylsulfonates, the alkyl and aryl groups of which preferably comprise from 1 to 20 carbon atoms and from 6 to 30 carbon atoms respectively, - the quaternary di- or tri-ammonium salts of formula (VIII): R 17 ^ 19 R i 6 —N— (CH 2 ) 3 - N— R 21 R R j8 20 (VIII) Formula (VIII) in which: - Ri6 denotes an alkyl group comprising approximately from 16 to 30 carbon atoms optionally hydroxylated and / or optionally interrupted by one or more oxygen atoms, - R17 denotes hydrogen, an alkyl group containing from 1 to 4 carbon atoms or a group - (CH 2 ) 3-N + (Ri6a) (Ri7a) (Ri8a), Ri6a, Ri7a, Risa, identical or different denoting hydrogen or an alkyl group containing from 1 to 4 carbon atoms, Ris, R19, R20 and R21, identical or different, denote hydrogen or an alkyl group containing from 1 to 4 carbon atoms, and - X 'is an anion chosen in particular from the group of halides, acetates, phosphates, nitrates, (Ci-C4) alkyl sulfates, (Ci-C4) alkyl sulfonates and (Ci-C4) alkyl aryl-sulfonates, in particular methyl sulfate ethyl sulfate, - quaternary ammonium salts containing one or more ester functions of formula (IX) below: θ (Ç S H 2S O) Z —r 25 r 2 — C - (- OC, H r2 (OH) r7 ^ —N ^ - (- C t H t2 (OH) ,, - O -) ^ R 23 (ix) Formula (IX) in which: - R22 is chosen from C 1 -C 6 alkyl groups and C 1 -C 6 hydroxyalkyl or dihydroxyalkyl groups, - R23 is chosen from the group R26-C (= O) -; linear or branched, saturated or unsaturated C1 to C22 hydrocarbon R27 groups; and the hydrogen atom, - R25 is chosen from the group R28-C (= O) -; linear or branched, saturated or unsaturated C1-C6 hydrocarbon groups R29; and the hydrogen atom, - R24, R26 and R28, identical or different, are chosen from C7-C21 hydrocarbon groups, linear or branched, saturated or unsaturated, - r, s and t, identical or different, are integers ranging from 2 to 6, - rl and tl, identical or different, are worth 0 or 1, - r2 and t2, identical or different, are integers such that r2 + rl = 2r and tl + t2 = 2t, - y is an integer from 1 to 10, - x and z, identical or different, are integers ranging from 0 to 10, it being understood that the sum x + y + z is worth from 1 to 15, - X 'is an anion, provided that when x = 0 then R23 denotes R27 and that when z = 0 then R25 denotes R29 · [7" id="c-fr-0007] 7. Method according to claim 6, characterized in that the first cationic surfactant (s) of the first composition and the second cationic surfactant (s) of the second composition are chosen, independently of one another, from those of formula (VI) or (IX), and mixtures of these compounds, and preferably among those of formula (VI), and mixtures of these compounds. [8" id="c-fr-0008] 8. Method according to any one of the preceding claims, characterized in that the first cationic surfactant (s) of the first composition and the second cationic surfactant (s) of the second composition are chosen, independently of one another, from the salts of cetyltrimethylammonium, behenyltrimethylammonium, dipalmitoylethylhydroxyethylmethylammonium, and mixtures thereof; and preferably among the cetyltrimethylammonium, behenyltrimethylammonium salts and their mixtures. [9" id="c-fr-0009] 9. Method according to any one of the preceding claims, characterized in that the first cationic surfactant (s) of the first composition represent a total content of 0.05 to 15% by weight, preferably 0.1 to 10% by weight. weight, and more preferably from 1 to 5% by weight, relative to the total weight of the first composition. [10" id="c-fr-0010] 10. Method according to any one of the preceding claims, characterized in that the second cationic surfactant (s) of the second composition represent a total content of 0.05 to 10% by weight, preferably 0.1 to 5% by weight. weight, and more preferably from 0.5 to 2% by weight, relative to the total weight of the second composition. [11" id="c-fr-0011] 11. Method according to any one of the preceding claims, characterized in that the second composition comprises at least 15% by weight, preferably comprises at least 50% by weight, more preferably from 50 to 99.5% by weight, in particular from 70 to 99.5%, and even better from 80 to 99.5% by weight of water, relative to the total weight of the second composition. [12" id="c-fr-0012] 12. Method according to any one of the preceding claims, characterized in that the first and the second compositions are mixed in a first composition / second composition weight ratio ranging from 0.2 to 5, preferably ranging from 0.3 to 3 , more preferably ranging from 0.5 to 1.5, and in particular the weight ratio is equal to 1/1. [13" id="c-fr-0013] 13. Method according to any one of the preceding claims, characterized in that the mixing step is carried out just before the application step, preferably less than two hours before, more preferably less than an hour before, and even better less than 15 minutes before the application stage. [14" id="c-fr-0014] 14. Kit comprising at least two compartments: a first compartment comprising a first composition as defined in any one of claims 1 to 9, - a second compartment comprising a second composition as defined in any one of claims 1, 6 to 8, 10 and 11. [15" id="c-fr-0015] 15. Cosmetic composition for the cosmetic treatment of keratin fibers comprising: i) one or more non-amino oxyalkylenated silicones, preferably non-amino oxyethylenated silicones, ii) one or more first cationic surfactants, iii) one or more second cationic surfactants different from the cationic surfactants (ii), iv) of water. [16" id="c-fr-0016] 16. Cosmetic composition according to claim 15, characterized in that the silicone (s) (i) are as defined in claim 3 or 4, and / or the first cationic surfactant (s) (ii) are as defined in any one of claims 6 to 8, and / or the second cationic surfactant (s) (iii) are as defined in any one of claims 6 to 8.
类似技术:
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同族专利:
公开号 | 公开日 FR3064476B1|2020-10-23| CN110545789A|2019-12-06| US20200022902A1|2020-01-23| WO2018178341A1|2018-10-04| EP3600236A1|2020-02-05|
引用文献:
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quaternary ammonium compounds| US3929990A|1973-12-18|1975-12-30|Millmaster Onyx Corp|Microbiocidal polymeric quaternary ammonium compounds| US4005193A|1974-08-07|1977-01-25|Millmaster Onyx Corporation|Microbiocidal polymeric quaternary ammonium compounds| US4025627A|1973-12-18|1977-05-24|Millmaster Onyx Corporation|Microbiocidal polymeric quaternary ammonium compounds| US4025617A|1974-10-03|1977-05-24|Millmaster Onyx Corporation|Anti-microbial quaternary ammonium co-polymers| DK659674A|1974-01-25|1975-09-29|Calgon Corp| FR2280361B2|1974-08-02|1981-11-13|Oreal| US4027020A|1974-10-29|1977-05-31|Millmaster Onyx Corporation|Randomly terminated capped polymers| US4001432A|1974-10-29|1977-01-04|Millmaster Onyx Corporation|Method of inhibiting the growth of bacteria by the application thereto of capped polymers| AT365448B|1975-07-04|1982-01-11|Oreal|COSMETIC PREPARATION| CH599389B5|1975-12-23|1978-05-31|Ciba Geigy Ag| GB1567947A|1976-07-02|1980-05-21|Unilever Ltd|Esters of quaternised amino-alcohols for treating fabrics| FR2368508B2|1977-03-02|1982-12-03|Oreal| LU78153A1|1977-09-20|1979-05-25|Oreal|COSMETIC COMPOSITIONS BASED ON QUATERNARY POLYAMMONIUM POLYMERS AND PREPARATION PROCESS| LU83349A1|1981-05-08|1983-03-24|Oreal|AEROSOL FOAM COMPOSITION BASED ON CATIONIC POLYMER AND ANIONIC POLYMER| LU84708A1|1983-03-23|1984-11-14|Oreal|THICKENED OR GELLIED HAIR CONDITIONING COMPOSITION CONTAINING AT LEAST ONE CATIONIC POLYMER, AT LEAST ONE ANIONIC POLYMER AND AT LEAST ONE XANTHANE GUM| DE3375135D1|1983-04-15|1988-02-11|Miranol Inc|Polyquaternary ammonium compounds and cosmetic compositions containing them| DE3623215A1|1986-07-10|1988-01-21|Henkel Kgaa|NEW QUARTERS OF AMMONIUM COMPOUNDS AND THEIR USE| US5472686A|1990-12-28|1995-12-05|Nippon Unicar Company Limited|Cosmetic formulations| US5149765A|1990-06-27|1992-09-22|Siltech Inc.|Terminal phosphated silicone polymers| US5091493A|1990-06-27|1992-02-25|Siltech Inc.|Silicone phosphobetaines| US5093452A|1990-06-27|1992-03-03|Siltech Inc.|Silicone phosphate amines| US5070171A|1990-06-27|1991-12-03|Siltech Inc.|Phosphated silicone polymers| FR2673179B1|1991-02-21|1993-06-11|Oreal|CERAMIDES, THEIR PREPARATION PROCESS AND THEIR APPLICATIONS IN COSMETICS AND DERMOPHARMACY.| FR2751221B1|1996-07-17|1998-09-04|Oreal|PRESSURIZED COMPOSITION BASED ON FIXING POLYMER, SOLVENT AND OXYALKYLENATED SILICONE, AND RESULTING FOAM| FR2780408B1|1998-06-25|2000-07-28|Oreal|ANHYDROUS COMPOSITION, USE IN COSMETICS, PHARMACY OR HYGIENE| FR2794971B1|1999-06-18|2003-08-29|Oreal|HAIR COSMETIC COMPOSITION IN THE FORM OF A WATER-IN-SILICONE EMULSION COMPRISING AT LEAST ONE FIXING POLYMER| FR2829387B1|2001-09-11|2005-08-26|Oreal|COSMETIC COMPOSITIONS CONTAINING A METHACRYLIC ACID COPOLYMER, A DIMETHICONE AND A CATIONIC POLYMER AND USES THEREOF| CN100471482C|2003-09-17|2009-03-25|荷兰联合利华有限公司|Hair care composition| EP2293766A2|2008-06-25|2011-03-16|The Procter & Gamble Company|Hair conditioning composition containing behenyl trimethyl ammonium chloride, and having higher yield point| CN101697940B|2009-11-10|2012-11-21|广州市迪彩化妆品有限公司|Hair care composition and preparation method thereof|JP2022516525A|2018-12-31|2022-02-28|ロレアル|Hair care and conditioning composition| WO2021222513A1|2020-04-30|2021-11-04|L'oreal|Hair treatment compositions| US11058618B1|2020-04-30|2021-07-13|L'oreal|Hair treatment compositions| FR3111548A1|2020-06-18|2021-12-24|L'oreal|HAIR TREATMENT COMPOSITIONS| DE102020123257A1|2020-09-07|2022-03-10|Henkel Ag & Co. Kgaa|CLEAR LIQUID HAIR MASK WITH CONSISTENCY TRANSFORMATION AND IMMEDIATE EFFECT DURING APPLICATION|
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2018-02-23| PLFP| Fee payment|Year of fee payment: 2 | 2018-10-05| PLSC| Publication of the preliminary search report|Effective date: 20181005 | 2019-02-13| PLFP| Fee payment|Year of fee payment: 3 | 2020-02-14| PLFP| Fee payment|Year of fee payment: 4 | 2021-02-10| PLFP| Fee payment|Year of fee payment: 5 | 2022-02-10| PLFP| Fee payment|Year of fee payment: 6 |
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申请号 | 申请日 | 专利标题 FR1752806A|FR3064476B1|2017-03-31|2017-03-31|COSMETIC TREATMENT PROCESS FOR KERATINIC FIBERS INCLUDING THE APPLICATION OF A BASE COMPOSITION AND OF A COMPOSITION INCLUDING A CATIONIC SURFACTANT| FR1752806|2017-03-31|FR1752806A| FR3064476B1|2017-03-31|2017-03-31|COSMETIC TREATMENT PROCESS FOR KERATINIC FIBERS INCLUDING THE APPLICATION OF A BASE COMPOSITION AND OF A COMPOSITION INCLUDING A CATIONIC SURFACTANT| EP18715021.4A| EP3600236A1|2017-03-31|2018-03-30|Cosmetic process for treating keratin fibres, comprising the application of a base composition and a composition comprising a cationic surfactant| US16/497,577| US20200022902A1|2017-03-31|2018-03-30|Cosmetic process for treating keratin fibres, comprising the application of a base composition and a composition comprising a cationic surfactant| CN201880023177.XA| CN110545789A|2017-03-31|2018-03-30|cosmetic method for treating keratin fibres comprising the application of a base composition and a composition comprising a cationic surfactant| PCT/EP2018/058304| WO2018178341A1|2017-03-31|2018-03-30|Cosmetic process for treating keratin fibres, comprising the application of a base composition and a composition comprising a cationic surfactant| 相关专利
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